A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv437818



Internal ID15383124
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr17:35715958..35716365hg38UCSC Ensembl
Outerchr17:35715312..35724157hg38UCSC Ensembl
Innerchr17:34042977..34043384hg19UCSC Ensembl
Outerchr17:34042331..34051176hg19UCSC Ensembl
Innerchr17:31067090..31067497hg18UCSC Ensembl
Outerchr17:31066444..31075289hg18UCSC Ensembl
Innerchr17:34188527..34188934hg16UCSC Ensembl
Outerchr17:34187881..34196726hg16UCSC Ensembl
Cytoband17q12
Allele length
AssemblyAllele length
hg388846
hg198846
hg188846
hg168846
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv52n17
Supporting Variantsnssv467699
SamplesNA19194
Known GenesAP2B1
MethodSNP array
AnalysisOur algorithm aims to detect deletions that are transmitted from a hemizygous parent to a child. For each trio, every SNP was coded into one of seven categories: (A) Type I mendelian incompatibility (that is, consistent with deletion) involving mother; (B) Type I mendelian incompatibility involving father; (C) Type II mendelian incompatibility (that is, inconsistent with deletion); (D) child homozygous or missing data, both parents homozygous or missing data; (E) child homozygous or missing data, father heterozygous, mother homozygous or missing data; (F) child homozygous or missing data, mother heterozygous, father homozygous or missing data; (G) child heterozygous or both parents heterozygous (see Supplementary Methods for further details). SNPs were assigned to states D-G only if they did not contain mendelian incompatibilities. A run of consecutive SNPs in a particular trio was considered to be consistent with a maternal transmitted deletion if all SNPs were in states A, D or E, or with a paternal deletion if all SNPs were in states B, D or F.
PlatformNot reported
Comments
ReferenceConrad_et_al_2006
Pubmed ID16327808
Accession Number(s)nsv437818
Frequency
Sample Size60
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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