A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1057076



Internal ID19146295
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr19:54218406..54250521hg38UCSC Ensembl
Innerchr19:54722275..54754385hg19UCSC Ensembl
Innerchr19:59414087..59446197hg18UCSC Ensembl
Cytoband19q13.42
Allele length
AssemblyAllele length
hg3832116
hg1932111
hg1832111
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv3573332
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)nsv1057076
Frequency
Sample Size11257
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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