A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1063490



Internal ID19152709
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr19:42866463..43033226hg38UCSC Ensembl
Innerchr19:43370615..43537378hg19UCSC Ensembl
Innerchr19:48062455..48229218hg18UCSC Ensembl
Cytoband19q13.2
Allele length
AssemblyAllele length
hg38166764
hg19166764
hg18166764
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv3575n100
Supporting Variantsnssv3570141
Samples
Known GenesPSG1, PSG11, PSG6, PSG7
MethodSNP array
AnalysisAffymetrix SNP array copy number analysis
PlatformAffymetrix SNP Array 6.0
Comments
ReferenceCoe_et_al_2014
Pubmed ID25217958
Accession Number(s)nsv1063490
Frequency
Sample Size11257
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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