A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv516566



Internal ID15443859
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr19:495722..525739hg38UCSC Ensembl
Innerchr19:495722..525739hg19UCSC Ensembl
Innerchr19:446722..476739hg18UCSC Ensembl
Innerchr19:446722..476739hg17UCSC Ensembl
Cytoband19p13.3
Allele length
AssemblyAllele length
hg3830018
hg1930018
hg1830018
hg1730018
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv677303, nssv660354, nssv669213
Samples
Known GenesMADCAM1, TPGS1
MethodSNP array
AnalysisSample-level CNVs
PlatformGPL6434
Comments
ReferenceShaikh_et_al_2009
Pubmed ID19592680
Accession Number(s)nsv516566
Frequency
Sample Size2026
Observed Gain3
Observed Loss0
Observed Complex0
Frequencyn/a


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