A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv606814



Internal ID16394223
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr7:44960264..44961564hg38UCSC Ensembl
Innerchr7:44999863..45001163hg19UCSC Ensembl
Innerchr7:44966388..44967688hg18UCSC Ensembl
Cytoband7p13
Allele length
AssemblyAllele length
hg381301
hg191301
hg181301
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv1083565
Samples
Known Genes
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)nsv606814
Frequency
Sample Size17421
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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