A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1063619



Internal ID19152838
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr19:43052691..43106905hg38UCSC Ensembl
Innerchr19:43556843..43611057hg19UCSC Ensembl
Innerchr19:48248683..48302897hg18UCSC Ensembl
Cytoband19q13.31
Allele length
AssemblyAllele length
hg3854215
hg1954215
hg1854215
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv3586n100
Supporting Variantsnssv3723067, nssv3571791
Samples
Known GenesPSG2
MethodSNP array
AnalysisAffymetrix SNP array copy number analysis
PlatformAffymetrix SNP Array 6.0
Comments
ReferenceCoe_et_al_2014
Pubmed ID25217958
Accession Number(s)nsv1063619
Frequency
Sample Size11257
Observed Gain0
Observed Loss2
Observed Complex0
Frequencyn/a


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