A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv525977



Internal ID15106584
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr19:11193728..11247764hg38UCSC Ensembl
Innerchr19:11304404..11358440hg19UCSC Ensembl
Innerchr19:11165404..11219440hg18UCSC Ensembl
Innerchr19:11165404..11219440hg17UCSC Ensembl
Cytoband19p13.2
Allele length
AssemblyAllele length
hg3854037
hg1954037
hg1854037
hg1754037
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv702196
Samples
Known GenesC19orf80, DOCK6, KANK2
MethodSNP array
AnalysisSample-level CNVs
PlatformGPL6434
Comments
ReferenceShaikh_et_al_2009
Pubmed ID19592680
Accession Number(s)nsv525977
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