A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv3574936



Internal ID18526531
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr19:48027173..48081406hg38UCSC Ensembl
Innerchr19:48530430..48584663hg19UCSC Ensembl
Innerchr19:53222242..53276475hg18UCSC Ensembl
Cytoband19q13.32
Allele length
AssemblyAllele length
hg3854234
hg1954234
hg1854234
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv1056392
Supporting Variants
Samples
Known GenesCABP5, PLA2G4C
MethodSNP array
AnalysisAffymetrix SNP array copy number analysis
PlatformAffymetrix SNP Array 6.0
Comments
ReferenceCoe_et_al_2014
Pubmed ID25217958
Accession Number(s)nssv3574936
Frequency
Sample Size29084
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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