A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1060095



Internal ID19149314
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr19:43000404..43252073hg38UCSC Ensembl
Innerchr19:43504556..43756225hg19UCSC Ensembl
Innerchr19:48196396..48448065hg18UCSC Ensembl
Cytoband19q13.31
Allele length
AssemblyAllele length
hg38251670
hg19251670
hg18251670
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv3583n100
Supporting Variantsnssv3571662, nssv3570215, nssv3571663
Samples
Known GenesLOC284344, PSG11, PSG2, PSG4, PSG5
MethodSNP array
AnalysisAffymetrix SNP array copy number analysis
PlatformAffymetrix SNP Array 6.0
Comments
ReferenceCoe_et_al_2014
Pubmed ID25217958
Accession Number(s)nsv1060095
Frequency
Sample Size11257
Observed Gain0
Observed Loss3
Observed Complex0
Frequencyn/a


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