A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv1084069



Internal ID15937255
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 StatusS
Merged Variantsnsv606937
Supporting Variants
Samples
Known Genes
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)nssv1084069
Frequency
Sample Size17421
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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