A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv3568183



Internal ID18866464
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr19:36387539..36457026hg38UCSC Ensembl
Innerchr19:36878441..36947928hg19UCSC Ensembl
Innerchr19:41570281..41639768hg18UCSC Ensembl
Cytoband19q13.12
Allele length
AssemblyAllele length
hg3869488
hg1969488
hg1869488
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv1066026
Supporting Variants
Samples
Known GenesLOC644189, ZFP82, ZNF566
MethodSNP array
AnalysisAffymetrix SNP array copy number analysis
PlatformAffymetrix SNP Array 6.0
Comments
ReferenceCoe_et_al_2014
Pubmed ID25217958
Accession Number(s)nssv3568183
Frequency
Sample Size11257
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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