A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv1009764



Internal ID15957034
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr4:159102626..159104226hg38UCSC Ensembl
Innerchr4:160023778..160025378hg19UCSC Ensembl
Innerchr4:160243228..160244828hg18UCSC Ensembl
Cytoband4q32.1
Allele length
AssemblyAllele length
hg381601
hg191601
hg181601
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv595810
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)nssv1009764
Frequency
Sample Size17421
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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