A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv520992



Internal ID15448285
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr6:142797578..142799222hg38UCSC Ensembl
Innerchr6:143118715..143120359hg19UCSC Ensembl
Innerchr6:143160408..143162052hg18UCSC Ensembl
Innerchr6:143160408..143162052hg17UCSC Ensembl
Cytoband6q24.2
Allele length
AssemblyAllele length
hg381645
hg191645
hg181645
hg171645
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv690167, nssv679446, nssv686609, nssv680360
Samples
Known GenesHIVEP2
MethodSNP array
AnalysisSample-level CNVs
PlatformGPL6434
Comments
ReferenceShaikh_et_al_2009
Pubmed ID19592680
Accession Number(s)nsv520992
Frequency
Sample Size2026
Observed Gain0
Observed Loss4
Observed Complex0
Frequencyn/a


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