A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv700553



Internal ID15437205
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr7:112828..113319hg38UCSC Ensembl
Innerchr7:112828..113319hg19UCSC Ensembl
Innerchr7:207911..208402hg18UCSC Ensembl
Innerchr7:207911..208402hg17UCSC Ensembl
Cytoband7p22.3
Allele length
AssemblyAllele length
hg38492
hg19492
hg18492
hg17492
Variant TypeCNV loss
Copy Number
Allele StateHeterozygous
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv516015
Supporting Variants
Samples
Known Genes
MethodSNP array
AnalysisSample-level CNVs
PlatformGPL6434
Comments
ReferenceShaikh_et_al_2009
Pubmed ID19592680
Accession Number(s)nssv700553
Frequency
Sample Size2026
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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