A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv607686



Internal ID16395095
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr7:81227880..81287832hg38UCSC Ensembl
Innerchr7:80857196..80917148hg19UCSC Ensembl
Innerchr7:80695132..80755084hg18UCSC Ensembl
Cytoband7q21.11
Allele length
AssemblyAllele length
hg3859953
hg1959953
hg1859953
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv1088538
Samples
Known Genes
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)nsv607686
Frequency
Sample Size17421
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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