A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv437793



Internal ID15383099
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr13:73450161..73450355hg38UCSC Ensembl
Outerchr13:73445237..73451292hg38UCSC Ensembl
Innerchr13:74024298..74024492hg19UCSC Ensembl
Outerchr13:74019374..74025429hg19UCSC Ensembl
Innerchr13:72922299..72922493hg18UCSC Ensembl
Outerchr13:72917375..72923430hg18UCSC Ensembl
Innerchr13:71822299..71822493hg16UCSC Ensembl
Outerchr13:71817375..71823430hg16UCSC Ensembl
Cytoband13q22.1
Allele length
AssemblyAllele length
hg386056
hg196056
hg186056
hg166056
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv46n17
Supporting Variantsnssv467674
SamplesNA19240
Known Genes
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)nsv437793
Frequency
Sample Size60
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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