A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv593901



Internal ID16381310
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr4:31752825..31807078hg38UCSC Ensembl
Innerchr4:31754447..31808700hg19UCSC Ensembl
Innerchr4:31363545..31417795hg18UCSC Ensembl
Cytoband4p15.1
Allele length
AssemblyAllele length
hg3854254
hg1954254
hg1854251
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv1152601
SamplesNINDS_147
Known Genes
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)nsv593901
Frequency
Sample Size17421
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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