A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1060759



Internal ID19149978
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 gain+loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv3659n100
Supporting Variantsnssv3573340, nssv3573339, nssv3573341
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)nsv1060759
Frequency
Sample Size11257
Observed Gain1
Observed Loss2
Observed Complex0
Frequencyn/a


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