A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv683177



Internal ID15419829
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr7:5477309..5532501hg38UCSC Ensembl
Innerchr7:5516940..5572132hg19UCSC Ensembl
Innerchr7:5483466..5538658hg18UCSC Ensembl
Innerchr7:5290181..5345373hg17UCSC Ensembl
Cytoband7p22.1
Allele length
AssemblyAllele length
hg3855193
hg1955193
hg1855193
hg1755193
Variant TypeCNV loss
Copy Number
Allele StateHeterozygous
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv517558
Supporting Variants
Samples
Known GenesACTB, FBXL18, MIR589
MethodSNP array
AnalysisSample-level CNVs
PlatformGPL6434
Comments
ReferenceShaikh_et_al_2009
Pubmed ID19592680
Accession Number(s)nssv683177
Frequency
Sample Size2026
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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