A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv525099



Internal ID15105706
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr7:156671417..156676926hg38UCSC Ensembl
Innerchr7:156464111..156469620hg19UCSC Ensembl
Innerchr7:156156872..156162381hg18UCSC Ensembl
Innerchr7:155963587..155969096hg17UCSC Ensembl
Cytoband7q36.3
Allele length
AssemblyAllele length
hg385510
hg195510
hg185510
hg175510
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv701158
Samples
Known GenesRNF32
MethodSNP array
AnalysisSample-level CNVs
PlatformGPL6434
Comments
ReferenceShaikh_et_al_2009
Pubmed ID19592680
Accession Number(s)nsv525099
Frequency
Sample Size2026
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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