A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1061041



Internal ID19150260
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr19:54640223..54664828hg38UCSC Ensembl
Innerchr19:55151674..55176279hg19UCSC Ensembl
Innerchr19:59843486..59868091hg18UCSC Ensembl
Cytoband19q13.42
Allele length
AssemblyAllele length
hg3824606
hg1924606
hg1824606
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv3573431
Samples
Known GenesLILRB4, MIR8061
MethodSNP array
AnalysisAffymetrix SNP array copy number analysis
PlatformAffymetrix SNP Array 6.0
Comments
ReferenceCoe_et_al_2014
Pubmed ID25217958
Accession Number(s)nsv1061041
Frequency
Sample Size11257
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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