A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv3566526



Internal ID18864807
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr19:28718948..28752848hg38UCSC Ensembl
Innerchr19:29209855..29243755hg19UCSC Ensembl
Innerchr19:33901695..33935595hg18UCSC Ensembl
Cytoband19q12
Allele length
AssemblyAllele length
hg3833901
hg1933901
hg1833901
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv1058756
Supporting Variants
Samples
Known Genes
MethodSNP array
AnalysisAffymetrix SNP array copy number analysis
PlatformAffymetrix SNP Array 6.0
Comments
ReferenceCoe_et_al_2014
Pubmed ID25217958
Accession Number(s)nssv3566526
Frequency
Sample Size11257
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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