A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv3564781



Internal ID18516376
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr19:15166388..15189458hg38UCSC Ensembl
Innerchr19:15277199..15300269hg19UCSC Ensembl
Innerchr19:15138199..15161269hg18UCSC Ensembl
Cytoband19p13.12
Allele length
AssemblyAllele length
hg3823071
hg1923071
hg1823071
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv1056996
Supporting Variants
Samples
Known GenesMIR6795, NOTCH3
MethodSNP array
AnalysisAffymetrix SNP array copy number analysis
PlatformAffymetrix SNP Array 6.0
Comments
ReferenceCoe_et_al_2014
Pubmed ID25217958
Accession Number(s)nssv3564781
Frequency
Sample Size29084
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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