A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv607708



Internal ID16395117
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr7:83866564..83897427hg38UCSC Ensembl
Innerchr7:83495880..83526743hg19UCSC Ensembl
Innerchr7:83333816..83364679hg18UCSC Ensembl
Cytoband7q21.11
Allele length
AssemblyAllele length
hg3830864
hg1930864
hg1830864
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv11487n54
Supporting Variantsnssv1089369
Samples
Known Genes
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)nsv607708
Frequency
Sample Size17421
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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