A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv673099



Internal ID15063065
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr7:65219183..65491268hg38UCSC Ensembl
Innerchr7:64679561..64956181hg19UCSC Ensembl
Innerchr7:64316996..64593616hg18UCSC Ensembl
Innerchr7:64123711..64400331hg17UCSC Ensembl
Cytoband7q11.21
Allele length
AssemblyAllele length
hg38272086
hg19276621
hg18276621
hg17276621
Variant TypeCNV loss
Copy Number
Allele StateHeterozygous
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv517778
Supporting Variants
Samples
Known GenesZNF92
MethodSNP array
AnalysisSample-level CNVs
PlatformGPL6434
Comments
ReferenceShaikh_et_al_2009
Pubmed ID19592680
Accession Number(s)nssv673099
Frequency
Sample Size2026
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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