A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv521605



Internal ID15448898
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr19:36770908..36992542hg38UCSC Ensembl
Innerchr19:37261810..37483444hg19UCSC Ensembl
Innerchr19:41953650..42175284hg18UCSC Ensembl
Innerchr19:41953650..42175284hg17UCSC Ensembl
Cytoband19q13.12
Allele length
AssemblyAllele length
hg38221635
hg19221635
hg18221635
hg17221635
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv698221
Samples
Known GenesZNF345, ZNF568, ZNF790, ZNF790-AS1, ZNF829, ZNF850
MethodSNP array
AnalysisSample-level CNVs
PlatformGPL6434
Comments
ReferenceShaikh_et_al_2009
Pubmed ID19592680
Accession Number(s)nsv521605
Frequency
Sample Size2026
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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