A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1061096



Internal ID19150315
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr19:54215071..54237431hg38UCSC Ensembl
Innerchr19:54718940..54741307hg19UCSC Ensembl
Innerchr19:59410752..59433119hg18UCSC Ensembl
Cytoband19q13.42
Allele length
AssemblyAllele length
hg3822361
hg1922368
hg1822368
Variant TypeCNV gain+loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv3573322, nssv3573324, nssv3726551, nssv3573325, nssv3573326, nssv3726552, nssv3573321, nssv3573323
Samples
Known GenesLILRA6, LILRB3
MethodSNP array
AnalysisAffymetrix SNP array copy number analysis
PlatformAffymetrix SNP Array 6.0
Comments
ReferenceCoe_et_al_2014
Pubmed ID25217958
Accession Number(s)nsv1061096
Frequency
Sample Size11257
Observed Gain1
Observed Loss7
Observed Complex0
Frequencyn/a


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