A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv686988



Internal ID15423640
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr7:38278989..38279738hg38UCSC Ensembl
Innerchr7:38318590..38319339hg19UCSC Ensembl
Innerchr7:38285115..38285864hg18UCSC Ensembl
Innerchr7:38091830..38092579hg17UCSC Ensembl
Cytoband7p14.1
Allele length
AssemblyAllele length
hg38750
hg19750
hg18750
hg17750
Variant TypeCNV loss
Copy Number
Allele StateHeterozygous
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv519863
Supporting Variants
Samples
Known Genes
MethodSNP array
AnalysisSample-level CNVs
PlatformGPL6434
Comments
ReferenceShaikh_et_al_2009
Pubmed ID19592680
Accession Number(s)nssv686988
Frequency
Sample Size2026
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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