A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv1077597



Internal ID15930783
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr7:20403..94119hg38UCSC Ensembl
Innerchr7:20403..94119hg19UCSC Ensembl
Innerchr7:113336..189202hg18UCSC Ensembl
Cytoband7p22.3
Allele length
AssemblyAllele length
hg3873717
hg1973717
hg1875867
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv605585
Supporting Variants
Samples
Known Genes
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)nssv1077597
Frequency
Sample Size17421
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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