A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv1079628



Internal ID15586128
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr7:16813184..16964677hg38UCSC Ensembl
Innerchr7:16852808..17004301hg19UCSC Ensembl
Innerchr7:16819333..16970826hg18UCSC Ensembl
Cytoband7p21.1
Allele length
AssemblyAllele length
hg38151494
hg19151494
hg18151494
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv606339
Supporting Variants
Samples
Known GenesAGR3
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)nssv1079628
Frequency
Sample Size17421
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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