A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv3564601



Internal ID18516196
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr19:1228266..1329640hg38UCSC Ensembl
Innerchr19:1228265..1329639hg19UCSC Ensembl
Innerchr19:1179265..1280639hg18UCSC Ensembl
Cytoband19p13.3
Allele length
AssemblyAllele length
hg38101375
hg19101375
hg18101375
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv1060536
Supporting Variants
Samples
Known GenesATP5D, C19orf24, C19orf26, CIRBP, CIRBP-AS1, EFNA2, MIDN, STK11
MethodSNP array
AnalysisAffymetrix SNP array copy number analysis
PlatformAffymetrix SNP Array 6.0
Comments
ReferenceCoe_et_al_2014
Pubmed ID25217958
Accession Number(s)nssv3564601
Frequency
Sample Size29084
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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