A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv3573341



Internal ID18871622
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr19:54226329..54249685hg38UCSC Ensembl
Innerchr19:54730202..54753543hg19UCSC Ensembl
Innerchr19:59422014..59445355hg18UCSC Ensembl
Cytoband19q13.42
Allele length
AssemblyAllele length
hg3823357
hg1923342
hg1823342
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv1060759
Supporting Variants
Samples
Known GenesLILRA6
MethodSNP array
AnalysisAffymetrix SNP array copy number analysis
PlatformAffymetrix SNP Array 6.0
Comments
ReferenceCoe_et_al_2014
Pubmed ID25217958
Accession Number(s)nssv3573341
Frequency
Sample Size11257
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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