A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv3722789



Internal ID18674384
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr19:42733612..42873123hg38UCSC Ensembl
Innerchr19:43237764..43377275hg19UCSC Ensembl
Innerchr19:47929604..48069115hg18UCSC Ensembl
Cytoband19q13.2
Allele length
AssemblyAllele length
hg38139512
hg19139512
hg18139512
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv1055408
Supporting Variants
Samples
Known GenesLOC100289650, PSG1, PSG10P, PSG3, PSG8
MethodSNP array
AnalysisAffymetrix SNP array copy number analysis
PlatformAffymetrix SNP Array 6.0
Comments
ReferenceCoe_et_al_2014
Pubmed ID25217958
Accession Number(s)nssv3722789
Frequency
Sample Size29084
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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