A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv527399



Internal ID15454692
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr7:75721820..75750787hg38UCSC Ensembl
Innerchr7:75351138..75380105hg19UCSC Ensembl
Innerchr7:75189074..75218041hg18UCSC Ensembl
Innerchr7:74995789..75024756hg17UCSC Ensembl
Cytoband7q11.23
Allele length
AssemblyAllele length
hg3828968
hg1928968
hg1828968
hg1728968
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv703835
Samples
Known GenesHIP1
MethodSNP array
AnalysisSample-level CNVs
PlatformGPL6434
Comments
ReferenceShaikh_et_al_2009
Pubmed ID19592680
Accession Number(s)nsv527399
Frequency
Sample Size2026
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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