A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv681385



Internal ID15418037
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr7:20183522..20185442hg38UCSC Ensembl
Innerchr7:20223145..20225065hg19UCSC Ensembl
Innerchr7:20189670..20191590hg18UCSC Ensembl
Innerchr7:19996385..19998305hg17UCSC Ensembl
Cytoband7p15.3
Allele length
AssemblyAllele length
hg381921
hg191921
hg181921
hg171921
Variant TypeCNV loss
Copy Number
Allele StateHeterozygous
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv520265
Supporting Variants
Samples
Known GenesMACC1
MethodSNP array
AnalysisSample-level CNVs
PlatformGPL6434
Comments
ReferenceShaikh_et_al_2009
Pubmed ID19592680
Accession Number(s)nssv681385
Frequency
Sample Size2026
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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