A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv520155



Internal ID15447448
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr19:57770006..57819644hg38UCSC Ensembl
Innerchr19:58281374..58331012hg19UCSC Ensembl
Innerchr19:62973186..63022824hg18UCSC Ensembl
Innerchr19:62973186..63022824hg17UCSC Ensembl
Cytoband19q13.43
Allele length
AssemblyAllele length
hg3849639
hg1949639
hg1849639
hg1749639
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv695605, nssv661276, nssv676862
Samples
Known GenesZNF552, ZNF586
MethodSNP array
AnalysisSample-level CNVs
PlatformGPL6434
Comments
ReferenceShaikh_et_al_2009
Pubmed ID19592680
Accession Number(s)nsv520155
Frequency
Sample Size2026
Observed Gain0
Observed Loss3
Observed Complex0
Frequencyn/a


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