A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv3569521



Internal ID18867802
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr19:42790226..43288527hg38UCSC Ensembl
Innerchr19:43294378..43792679hg19UCSC Ensembl
Innerchr19:47986218..48484519hg18UCSC Ensembl
Cytoband19q13.2
Allele length
AssemblyAllele length
hg38498302
hg19498302
hg18498302
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv1059067
Supporting Variants
Samples
Known GenesLOC100289650, LOC284344, PSG1, PSG10P, PSG11, PSG2, PSG4, PSG5, PSG6, PSG7, PSG9
MethodSNP array
AnalysisAffymetrix SNP array copy number analysis
PlatformAffymetrix SNP Array 6.0
Comments
ReferenceCoe_et_al_2014
Pubmed ID25217958
Accession Number(s)nssv3569521
Frequency
Sample Size11257
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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