A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv699501



Internal ID15089467
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr19:45515882..45526896hg38UCSC Ensembl
Innerchr19:46019140..46030154hg19UCSC Ensembl
Innerchr19:50710980..50721994hg18UCSC Ensembl
Innerchr19:50710980..50721994hg17UCSC Ensembl
Cytoband19q13.32
Allele length
AssemblyAllele length
hg3811015
hg1911015
hg1811015
hg1711015
Variant TypeCNV loss
Copy Number
Allele StateHeterozygous
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv523694
Supporting Variants
Samples
Known GenesVASP
MethodSNP array
AnalysisSample-level CNVs
PlatformGPL6434
Comments
ReferenceShaikh_et_al_2009
Pubmed ID19592680
Accession Number(s)nssv699501
Frequency
Sample Size2026
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


Hosted by The Centre for Applied Genomics
Grant support for DGV
Please read the usage disclaimer