A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv606937



Internal ID16394346
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr7:51526792..51534160hg38UCSC Ensembl
Innerchr7:51594489..51601857hg19UCSC Ensembl
Innerchr7:51561983..51569351hg18UCSC Ensembl
Cytoband7p12.1
Allele length
AssemblyAllele length
hg387369
hg197369
hg187369
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv11337n54
Supporting Variantsnssv1084069
Samples
Known Genes
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)nsv606937
Frequency
Sample Size17421
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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