A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv1152585



Internal ID15873966
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr4:4326185..4344700hg38UCSC Ensembl
Innerchr4:4327912..4346427hg19UCSC Ensembl
Innerchr4:4378813..4397328hg18UCSC Ensembl
Cytoband4p16.2
Allele length
AssemblyAllele length
hg3818516
hg1918516
hg1818516
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv593475
Supporting Variants
SamplesHGDP00451
Known Genes
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)nssv1152585
Frequency
Sample Size17421
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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