A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv609420



Internal ID16050143
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr7:158818315..159076724hg38UCSC Ensembl
Innerchr7:158611006..158869415hg19UCSC Ensembl
Innerchr7:158303767..158562176hg18UCSC Ensembl
Cytoband7q36.3
Allele length
AssemblyAllele length
hg38258410
hg19258410
hg18258410
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv11804n54
Supporting Variantsnssv1102022
Samples
Known GenesESYT2, LINC00689, VIPR2, WDR60
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)nsv609420
Frequency
Sample Size17421
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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