A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1059987



Internal ID19149206
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr19:43052691..43103053hg38UCSC Ensembl
Innerchr19:43556843..43607205hg19UCSC Ensembl
Innerchr19:48248683..48299045hg18UCSC Ensembl
Cytoband19q13.31
Allele length
AssemblyAllele length
hg3850363
hg1950363
hg1850363
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv3586n100
Supporting Variantsnssv3571790
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)nsv1059987
Frequency
Sample Size11257
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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