A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1061698



Internal ID19150917
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr19:54218406..54257872hg38UCSC Ensembl
Innerchr19:54722275..54761735hg19UCSC Ensembl
Innerchr19:59414087..59453547hg18UCSC Ensembl
Cytoband19q13.42
Allele length
AssemblyAllele length
hg3839467
hg1939461
hg1839461
Variant TypeCNV gain+loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv3658n100
Supporting Variantsnssv3573334, nssv3573335, nssv3573333, nssv3726555
Samples
Known GenesLILRA6, LILRB3, LILRB5
MethodSNP array
AnalysisAffymetrix SNP array copy number analysis
PlatformAffymetrix SNP Array 6.0
Comments
ReferenceCoe_et_al_2014
Pubmed ID25217958
Accession Number(s)nsv1061698
Frequency
Sample Size11257
Observed Gain1
Observed Loss3
Observed Complex0
Frequencyn/a


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