A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv605873



Internal ID16046596
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr7:2880433..3164544hg38UCSC Ensembl
Innerchr7:2920067..3204177hg19UCSC Ensembl
Innerchr7:2886593..3170703hg18UCSC Ensembl
Cytoband7p22.2
Allele length
AssemblyAllele length
hg38284112
hg19284111
hg18284111
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv1078477
Samples
Known GenesCARD11
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)nsv605873
Frequency
Sample Size17421
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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