A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv607709



Internal ID16395118
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr7:83866564..83904638hg38UCSC Ensembl
Innerchr7:83495880..83533954hg19UCSC Ensembl
Innerchr7:83333816..83371890hg18UCSC Ensembl
Cytoband7q21.11
Allele length
AssemblyAllele length
hg3838075
hg1938075
hg1838075
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv11487n54
Supporting Variantsnssv1089370
Samples
Known Genes
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)nsv607709
Frequency
Sample Size17421
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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