A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv1150158



Internal ID15855994
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr19:53097592..53122859hg38UCSC Ensembl
Innerchr19:53600845..53626112hg19UCSC Ensembl
Innerchr19:58292657..58317924hg18UCSC Ensembl
Cytoband19q13.41
Allele length
AssemblyAllele length
hg3825268
hg1925268
hg1825268
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv580070
Supporting Variants
Samples1798860292_A
Known GenesZNF160, ZNF415
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)nssv1150158
Frequency
Sample Size17421
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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