A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv608425



Internal ID16395834
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr7:131838027..131861757hg38UCSC Ensembl
Innerchr7:131522786..131546516hg19UCSC Ensembl
Innerchr7:131173326..131197056hg18UCSC Ensembl
Cytoband7q32.3
Allele length
AssemblyAllele length
hg3823731
hg1923731
hg1823731
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv1155230
SamplesHGDP00830
Known Genes
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)nsv608425
Frequency
Sample Size17421
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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