A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv1155128



Internal ID15530846
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr7:3915884..4573976hg38UCSC Ensembl
Innerchr7:3955516..4613607hg19UCSC Ensembl
Innerchr7:3922042..4580133hg18UCSC Ensembl
Cytoband7p22.1
Allele length
AssemblyAllele length
hg38658093
hg19658092
hg18658092
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv605939
Supporting Variants
SamplesHGDP01003
Known GenesSDK1
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)nssv1155128
Frequency
Sample Size17421
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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