A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1066188



Internal ID19155407
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr19:54226329..54257872hg38UCSC Ensembl
Innerchr19:54730202..54761735hg19UCSC Ensembl
Innerchr19:59422014..59453547hg18UCSC Ensembl
Cytoband19q13.42
Allele length
AssemblyAllele length
hg3831544
hg1931534
hg1831534
Variant TypeCNV gain+loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv3658n100
Supporting Variantsnssv3573383, nssv3573378, nssv3573373, nssv3573382, nssv3573371, nssv3573377, nssv3573381, nssv3573375, nssv3573380, nssv3573379, nssv3573374, nssv3726558, nssv3573372, nssv3573376, nssv3573384, nssv3573370
Samples
Known GenesLILRA6, LILRB5
MethodSNP array
AnalysisAffymetrix SNP array copy number analysis
PlatformAffymetrix SNP Array 6.0
Comments
ReferenceCoe_et_al_2014
Pubmed ID25217958
Accession Number(s)nsv1066188
Frequency
Sample Size11257
Observed Gain14
Observed Loss2
Observed Complex0
Frequencyn/a


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