A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1063373



Internal ID19152592
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr19:42978334..43134103hg38UCSC Ensembl
Innerchr19:43482486..43638255hg19UCSC Ensembl
Innerchr19:48174326..48330095hg18UCSC Ensembl
Cytoband19q13.31
Allele length
AssemblyAllele length
hg38155770
hg19155770
hg18155770
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv3581n100
Supporting Variantsnssv3570193
Samples
Known GenesPSG11, PSG2
MethodSNP array
AnalysisAffymetrix SNP array copy number analysis
PlatformAffymetrix SNP Array 6.0
Comments
ReferenceCoe_et_al_2014
Pubmed ID25217958
Accession Number(s)nsv1063373
Frequency
Sample Size11257
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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