A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv658834



Internal ID15048800
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr7:65001948..65451324hg38UCSC Ensembl
Innerchr7:64462326..64916237hg19UCSC Ensembl
Innerchr7:64099761..64553672hg18UCSC Ensembl
Innerchr7:63906476..64360387hg17UCSC Ensembl
Cytoband7q11.21
Allele length
AssemblyAllele length
hg38449377
hg19453912
hg18453912
hg17453912
Variant TypeCNV loss
Copy Number
Allele StateHeterozygous
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv517778
Supporting Variants
Samples
Known GenesCCT6P3, ERV3-1, ZNF92
MethodSNP array
AnalysisSample-level CNVs
PlatformGPL6434
Comments
ReferenceShaikh_et_al_2009
Pubmed ID19592680
Accession Number(s)nssv658834
Frequency
Sample Size2026
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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