A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv606364



Internal ID16393773
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr7:20166070..20183522hg38UCSC Ensembl
Innerchr7:20205693..20223145hg19UCSC Ensembl
Innerchr7:20172218..20189670hg18UCSC Ensembl
Cytoband7p15.3
Allele length
AssemblyAllele length
hg3817453
hg1917453
hg1817453
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv1079653
Samples
Known GenesMACC1
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)nsv606364
Frequency
Sample Size17421
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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