A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv705004



Internal ID15441656
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr7:9574931..9745624hg38UCSC Ensembl
Innerchr7:9614561..9785253hg19UCSC Ensembl
Innerchr7:9581086..9751778hg18UCSC Ensembl
Innerchr7:9387801..9558493hg17UCSC Ensembl
Cytoband7p21.3
Allele length
AssemblyAllele length
hg38170694
hg19170693
hg18170693
hg17170693
Variant TypeCNV loss
Copy Number
Allele StateHeterozygous
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv528412
Supporting Variants
Samples
Known GenesPER4
MethodSNP array
AnalysisSample-level CNVs
PlatformGPL6434
Comments
ReferenceShaikh_et_al_2009
Pubmed ID19592680
Accession Number(s)nssv705004
Frequency
Sample Size2026
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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