A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv607428



Internal ID16048151
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr7:68061087..68323564hg38UCSC Ensembl
Innerchr7:67526074..67788551hg19UCSC Ensembl
Innerchr7:67163509..67426507hg18UCSC Ensembl
Cytoband7q11.22
Allele length
AssemblyAllele length
hg38262478
hg19262478
hg18262999
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv1085703
Samples
Known Genes
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)nsv607428
Frequency
Sample Size17421
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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