A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv527053



Internal ID15107660
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr19:53097592..53122859hg38UCSC Ensembl
Innerchr19:53600845..53626112hg19UCSC Ensembl
Innerchr19:58292657..58317924hg18UCSC Ensembl
Innerchr19:58292657..58317924hg17UCSC Ensembl
Cytoband19q13.41
Allele length
AssemblyAllele length
hg3825268
hg1925268
hg1825268
hg1725268
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv703429
Samples
Known GenesZNF160, ZNF415
MethodSNP array
AnalysisSample-level CNVs
PlatformGPL6434
Comments
ReferenceShaikh_et_al_2009
Pubmed ID19592680
Accession Number(s)nsv527053
Frequency
Sample Size2026
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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