A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv733907



Internal ID16027863
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr1:195257331..195415124hg38UCSC Ensembl
Innerchr1:195226461..195384254hg19UCSC Ensembl
Innerchr1:193493084..193650877hg18UCSC Ensembl
Cytoband1q31.3
Allele length
AssemblyAllele length
hg38157794
hg19157794
hg18157794
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv548712
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)nssv733907
Frequency
Sample Size17421
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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