A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv695619



Internal ID15432271
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr1:87427106..87437341hg38UCSC Ensembl
Innerchr1:87892789..87903024hg19UCSC Ensembl
Innerchr1:87665377..87675612hg18UCSC Ensembl
Innerchr1:87604810..87615045hg17UCSC Ensembl
Cytoband1p22.3
Allele length
AssemblyAllele length
hg3810236
hg1910236
hg1810236
hg1710236
Variant TypeCNV loss
Copy Number
Allele StateHeterozygous
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv518195
Supporting Variants
Samples
Known Genes
MethodSNP array
AnalysisSample-level CNVs
PlatformGPL6434
Comments
ReferenceShaikh_et_al_2009
Pubmed ID19592680
Accession Number(s)nssv695619
Frequency
Sample Size2026
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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