A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv606277



Internal ID16047000
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr7:13868202..13927752hg38UCSC Ensembl
Innerchr7:13907827..13967377hg19UCSC Ensembl
Innerchr7:13874352..13933902hg18UCSC Ensembl
Cytoband7p21.2
Allele length
AssemblyAllele length
hg3859551
hg1959551
hg1859551
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv1079279
Samples
Known GenesETV1
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)nsv606277
Frequency
Sample Size17421
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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