A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv698871



Internal ID15435523
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr19:33235469..33251464hg38UCSC Ensembl
Innerchr19:33726375..33742370hg19UCSC Ensembl
Innerchr19:38418215..38434210hg18UCSC Ensembl
Innerchr19:38418215..38434210hg17UCSC Ensembl
Cytoband19q13.11
Allele length
AssemblyAllele length
hg3815996
hg1915996
hg1815996
hg1715996
Variant TypeCNV loss
Copy Number
Allele StateHeterozygous
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv523161
Supporting Variants
Samples
Known Genes
MethodSNP array
AnalysisSample-level CNVs
PlatformGPL6434
Comments
ReferenceShaikh_et_al_2009
Pubmed ID19592680
Accession Number(s)nssv698871
Frequency
Sample Size2026
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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