A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv523620



Internal ID15104227
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr7:35679524..35720619hg38UCSC Ensembl
Innerchr7:35719134..35760229hg19UCSC Ensembl
Innerchr7:35685659..35726754hg18UCSC Ensembl
Innerchr7:35492374..35533469hg17UCSC Ensembl
Cytoband7p14.2
Allele length
AssemblyAllele length
hg3841096
hg1941096
hg1841096
hg1741096
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv419n21
Supporting Variantsnssv699417
Samples
Known GenesHERPUD2, LOC100506725
MethodSNP array
AnalysisSample-level CNVs
PlatformGPL6434
Comments
ReferenceShaikh_et_al_2009
Pubmed ID19592680
Accession Number(s)nsv523620
Frequency
Sample Size2026
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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