A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1062314



Internal ID19151533
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr19:54218406..54270335hg38UCSC Ensembl
Innerchr19:54722275..54774189hg19UCSC Ensembl
Innerchr19:59414087..59466001hg18UCSC Ensembl
Cytoband19q13.42
Allele length
AssemblyAllele length
hg3851930
hg1951915
hg1851915
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv3656n100
Supporting Variantsnssv3573337, nssv3573338
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)nsv1062314
Frequency
Sample Size11257
Observed Gain2
Observed Loss0
Observed Complex0
Frequencyn/a


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