A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv3570143



Internal ID18868424
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr19:42879062..43030742hg38UCSC Ensembl
Innerchr19:43383214..43534894hg19UCSC Ensembl
Innerchr19:48075054..48226734hg18UCSC Ensembl
Cytoband19q13.2
Allele length
AssemblyAllele length
hg38151681
hg19151681
hg18151681
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv1062763
Supporting Variants
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)nssv3570143
Frequency
Sample Size11257
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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