A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1064692



Internal ID19153911
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr19:54249470..54320705hg38UCSC Ensembl
Innerchr19:54753328..54831977hg19UCSC Ensembl
Innerchr19:59445140..59523789hg18UCSC Ensembl
Cytoband19q13.42
Allele length
AssemblyAllele length
hg3871236
hg1978650
hg1878650
Variant TypeCNV gain+loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv3661n100
Supporting Variantsnssv3573414, nssv3573415
Samples
Known GenesLILRA3, LILRA5, LILRB2, LILRB5, MIR4752
MethodSNP array
AnalysisAffymetrix SNP array copy number analysis
PlatformAffymetrix SNP Array 6.0
Comments
ReferenceCoe_et_al_2014
Pubmed ID25217958
Accession Number(s)nsv1064692
Frequency
Sample Size11257
Observed Gain1
Observed Loss1
Observed Complex0
Frequencyn/a


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