A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv528638



Internal ID15109245
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr19:2827302..2846559hg38UCSC Ensembl
Innerchr19:2827300..2846557hg19UCSC Ensembl
Innerchr19:2778300..2797557hg18UCSC Ensembl
Innerchr19:2778300..2797557hg17UCSC Ensembl
Cytoband19p13.3
Allele length
AssemblyAllele length
hg3819258
hg1919258
hg1819258
hg1719258
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv705269
Samples
Known GenesZNF554, ZNF555
MethodSNP array
AnalysisSample-level CNVs
PlatformGPL6434
Comments
ReferenceShaikh_et_al_2009
Pubmed ID19592680
Accession Number(s)nsv528638
Frequency
Sample Size2026
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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