A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1063508



Internal ID19152727
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr19:54226329..54250521hg38UCSC Ensembl
Innerchr19:54730202..54754385hg19UCSC Ensembl
Innerchr19:59422014..59446197hg18UCSC Ensembl
Cytoband19q13.42
Allele length
AssemblyAllele length
hg3824193
hg1924184
hg1824184
Variant TypeCNV gain+loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv3659n100
Supporting Variantsnssv3573358, nssv3573365, nssv3573361, nssv3726557, nssv3573357, nssv3573360, nssv3573363, nssv3573368, nssv3573367, nssv3573362, nssv3573364, nssv3726556, nssv3573369, nssv3573359, nssv3573366
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)nsv1063508
Frequency
Sample Size11257
Observed Gain13
Observed Loss2
Observed Complex0
Frequencyn/a


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