A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1066720



Internal ID19155939
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr19:43000404..43264030hg38UCSC Ensembl
Innerchr19:43504556..43768182hg19UCSC Ensembl
Innerchr19:48196396..48460022hg18UCSC Ensembl
Cytoband19q13.31
Allele length
AssemblyAllele length
hg38263627
hg19263627
hg18263627
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv3583n100
Supporting Variantsnssv3571664
Samples
Known GenesLOC284344, PSG11, PSG2, PSG4, PSG5, PSG9
MethodSNP array
AnalysisAffymetrix SNP array copy number analysis
PlatformAffymetrix SNP Array 6.0
Comments
ReferenceCoe_et_al_2014
Pubmed ID25217958
Accession Number(s)nsv1066720
Frequency
Sample Size11257
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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