A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv605874



Internal ID16046597
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr7:2926504..3275940hg38UCSC Ensembl
Innerchr7:2966138..3315572hg19UCSC Ensembl
Innerchr7:2932664..3282098hg18UCSC Ensembl
Cytoband7p22.2
Allele length
AssemblyAllele length
hg38349437
hg19349435
hg18349435
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv1155117
SamplesHGDP01333
Known GenesCARD11
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)nsv605874
Frequency
Sample Size17421
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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