A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv519379



Internal ID15099986
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr3:114236340..114236473hg38UCSC Ensembl
Innerchr3:113955187..113955320hg19UCSC Ensembl
Innerchr3:115437877..115438010hg18UCSC Ensembl
Innerchr3:115437877..115438010hg17UCSC Ensembl
Cytoband3q13.31
Allele length
AssemblyAllele length
hg38134
hg19134
hg18134
hg17134
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv694326
Samples
Known GenesZNF80
MethodSNP array
AnalysisSample-level CNVs
PlatformGPL6434
Comments
ReferenceShaikh_et_al_2009
Pubmed ID19592680
Accession Number(s)nsv519379
Frequency
Sample Size2026
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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