A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv609363



Internal ID16050086
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr7:158638215..159135878hg38UCSC Ensembl
Innerchr7:158430907..158928569hg19UCSC Ensembl
Innerchr7:158123668..158621330hg18UCSC Ensembl
Cytoband7q36.3
Allele length
AssemblyAllele length
hg38497664
hg19497663
hg18497663
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv1101694
Samples
Known GenesESYT2, LINC00689, NCAPG2, VIPR2, WDR60
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)nsv609363
Frequency
Sample Size17421
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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