A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv3568898



Internal ID18867179
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr19:42776064..42870449hg38UCSC Ensembl
Innerchr19:43280216..43374601hg19UCSC Ensembl
Innerchr19:47972056..48066441hg18UCSC Ensembl
Cytoband19q13.2
Allele length
AssemblyAllele length
hg3894386
hg1994386
hg1894386
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv1065255
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)nssv3568898
Frequency
Sample Size11257
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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