A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv607687



Internal ID16395096
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr7:81236837..81308729hg38UCSC Ensembl
Innerchr7:80866153..80938045hg19UCSC Ensembl
Innerchr7:80704089..80775981hg18UCSC Ensembl
Cytoband7q21.11
Allele length
AssemblyAllele length
hg3871893
hg1971893
hg1871893
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv11484n54
Supporting Variantsnssv1155218
Samples1780854261_A
Known Genes
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)nsv607687
Frequency
Sample Size17421
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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