A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv671794



Internal ID15061760
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr7:65219183..65476540hg38UCSC Ensembl
Innerchr7:64679561..64941453hg19UCSC Ensembl
Innerchr7:64316996..64578888hg18UCSC Ensembl
Innerchr7:64123711..64385603hg17UCSC Ensembl
Cytoband7q11.21
Allele length
AssemblyAllele length
hg38257358
hg19261893
hg18261893
hg17261893
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)nssv671794
Frequency
Sample Size2026
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


Hosted by The Centre for Applied Genomics
Grant support for DGV
Please read the usage disclaimer