A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv607712



Internal ID16395121
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr7:84546973..84689167hg38UCSC Ensembl
Innerchr7:84176289..84318483hg19UCSC Ensembl
Innerchr7:84014225..84156419hg18UCSC Ensembl
Cytoband7q21.11
Allele length
AssemblyAllele length
hg38142195
hg19142195
hg18142195
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv11488n54
Supporting Variantsnssv1089373
Samples
Known Genes
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)nsv607712
Frequency
Sample Size17421
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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