A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv1150185



Internal ID15853539
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr19:54227805..54255708hg38UCSC Ensembl
Innerchr19:54731679..54759571hg19UCSC Ensembl
Innerchr19:59423491..59451383hg18UCSC Ensembl
Cytoband19q13.42
Allele length
AssemblyAllele length
hg3827904
hg1927893
hg1827893
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv580191
Supporting Variants
Samples1780854264_A
Known GenesLILRA6, LILRB5
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)nssv1150185
Frequency
Sample Size17421
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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