A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv526993



Internal ID15454286
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr7:148609857..148611087hg38UCSC Ensembl
Innerchr7:148306949..148308179hg19UCSC Ensembl
Innerchr7:147937882..147939112hg18UCSC Ensembl
Innerchr7:147744597..147745827hg17UCSC Ensembl
Cytoband7q36.1
Allele length
AssemblyAllele length
hg381231
hg191231
hg181231
hg171231
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv703367
Samples
Known GenesC7orf33
MethodSNP array
AnalysisSample-level CNVs
PlatformGPL6434
Comments
ReferenceShaikh_et_al_2009
Pubmed ID19592680
Accession Number(s)nsv526993
Frequency
Sample Size2026
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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