A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv1153496



Internal ID15874378
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr4:102014745..102087555hg38UCSC Ensembl
Innerchr4:102935902..103008712hg19UCSC Ensembl
Innerchr4:103154925..103227735hg18UCSC Ensembl
Cytoband4q24
Allele length
AssemblyAllele length
hg3872811
hg1972811
hg1872811
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv594955
Supporting Variants
SamplesHGDP00531
Known GenesBANK1
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)nssv1153496
Frequency
Sample Size17421
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


Hosted by The Centre for Applied Genomics
Grant support for DGV
Please read the usage disclaimer