A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv579469



Internal ID16020192
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr19:37847097..37852828hg38UCSC Ensembl
Innerchr19:38337737..38343468hg19UCSC Ensembl
Innerchr19:43029577..43035308hg18UCSC Ensembl
Cytoband19q13.13
Allele length
AssemblyAllele length
hg385732
hg195732
hg185732
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv899164
Samples
Known GenesLOC100631378
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)nsv579469
Frequency
Sample Size17421
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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