A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv1152905



Internal ID15878187
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr4:25555935..25576647hg38UCSC Ensembl
Innerchr4:25557557..25578269hg19UCSC Ensembl
Innerchr4:25166655..25187367hg18UCSC Ensembl
Cytoband4p15.2
Allele length
AssemblyAllele length
hg3820713
hg1920713
hg1820713
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv593836
Supporting Variants
SamplesHGDP01153
Known Genes
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)nssv1152905
Frequency
Sample Size17421
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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