A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv662468



Internal ID15052434
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr19:34468026..34496475hg38UCSC Ensembl
Innerchr19:34958931..34987380hg19UCSC Ensembl
Innerchr19:39650771..39679220hg18UCSC Ensembl
Innerchr19:39650771..39679220hg17UCSC Ensembl
Cytoband19q13.11
Allele length
AssemblyAllele length
hg3828450
hg1928450
hg1828450
hg1728450
Variant TypeCNV loss
Copy Number
Allele StateHeterozygous
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv517392
Supporting Variants
Samples
Known GenesUBA2, WTIP
MethodSNP array
AnalysisSample-level CNVs
PlatformGPL6434
Comments
ReferenceShaikh_et_al_2009
Pubmed ID19592680
Accession Number(s)nssv662468
Frequency
Sample Size2026
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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