A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv437088



Internal ID15382394
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr9:38655272..38664563hg38UCSC Ensembl
Outerchr9:38652717..38685646hg38UCSC Ensembl
Innerchr9:38655269..38664560hg19UCSC Ensembl
Outerchr9:38652714..38685643hg19UCSC Ensembl
Innerchr9:38645269..38654560hg18UCSC Ensembl
Outerchr9:38642714..38675643hg18UCSC Ensembl
Innerchr9:38645269..38654560hg16UCSC Ensembl
Outerchr9:38642714..38675643hg16UCSC Ensembl
Cytoband9p13.1
Allele length
AssemblyAllele length
hg3832930
hg1932930
hg1832930
hg1632930
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv466969
SamplesNA12864
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)nsv437088
Frequency
Sample Size60
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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