A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv606278



Internal ID16047001
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr7:13891557..13919781hg38UCSC Ensembl
Innerchr7:13931182..13959406hg19UCSC Ensembl
Innerchr7:13897707..13925931hg18UCSC Ensembl
Cytoband7p21.2
Allele length
AssemblyAllele length
hg3828225
hg1928225
hg1828225
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv1079281, nssv1079280
Samples
Known GenesETV1
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)nsv606278
Frequency
Sample Size17421
Observed Gain0
Observed Loss2
Observed Complex0
Frequencyn/a


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