A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv3569014



Internal ID18867295
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr19:42790226..42874755hg38UCSC Ensembl
Innerchr19:43294378..43378907hg19UCSC Ensembl
Innerchr19:47986218..48070747hg18UCSC Ensembl
Cytoband19q13.2
Allele length
AssemblyAllele length
hg3884530
hg1984530
hg1884530
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv1058926
Supporting Variants
Samples
Known GenesLOC100289650, PSG1, PSG10P
MethodSNP array
AnalysisAffymetrix SNP array copy number analysis
PlatformAffymetrix SNP Array 6.0
Comments
ReferenceCoe_et_al_2014
Pubmed ID25217958
Accession Number(s)nssv3569014
Frequency
Sample Size11257
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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