A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv3570792



Internal ID18869073
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr19:27257073..27337756hg38UCSC Ensembl
Innerchr19:27747981..27828664hg19UCSC Ensembl
Innerchr19:32439821..32520504hg18UCSC Ensembl
Cytoband19q11
Allele length
AssemblyAllele length
hg3880684
hg1980684
hg1880684
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv1055375
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)nssv3570792
Frequency
Sample Size11257
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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