A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv990139



Internal ID15937409
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr4:6678850..6683347hg38UCSC Ensembl
Innerchr4:6680577..6685074hg19UCSC Ensembl
Innerchr4:6731478..6735975hg18UCSC Ensembl
Cytoband4p16.1
Allele length
AssemblyAllele length
hg384498
hg194498
hg184498
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv593505
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)nssv990139
Frequency
Sample Size17421
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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