A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1063149



Internal ID18805680
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr19:43554929..43583431hg38UCSC Ensembl
Innerchr19:44059081..44087583hg19UCSC Ensembl
Innerchr19:48750921..48779423hg18UCSC Ensembl
Cytoband19q13.31
Allele length
AssemblyAllele length
hg3828503
hg1928503
hg1828503
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv3573780
Samples
Known GenesPINLYP, XRCC1
MethodSNP array
AnalysisAffymetrix SNP array copy number analysis
PlatformAffymetrix SNP Array 6.0
Comments
ReferenceCoe_et_al_2014
Pubmed ID25217958
Accession Number(s)nsv1063149
Frequency
Sample Size29084
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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