A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1061991



Internal ID19151210
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr19:54226329..54265512hg38UCSC Ensembl
Innerchr19:54730202..54769366hg19UCSC Ensembl
Innerchr19:59422014..59461178hg18UCSC Ensembl
Cytoband19q13.42
Allele length
AssemblyAllele length
hg3839184
hg1939165
hg1839165
Variant TypeCNV gain+loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv3658n100
Supporting Variantsnssv3573385, nssv3573389, nssv3573386, nssv3573387, nssv3573388
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)nsv1061991
Frequency
Sample Size11257
Observed Gain4
Observed Loss1
Observed Complex0
Frequencyn/a


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