A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv517365



Internal ID15097972
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr19:56080920..56163179hg38UCSC Ensembl
Innerchr19:56592286..56674548hg19UCSC Ensembl
Innerchr19:61284098..61366360hg18UCSC Ensembl
Innerchr19:61284098..61366360hg17UCSC Ensembl
Cytoband19q13.42
Allele length
AssemblyAllele length
hg3882260
hg1982263
hg1882263
hg1782263
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv207n21
Supporting Variantsnssv666756, nssv683167, nssv677473, nssv672625, nssv673343, nssv671054, nssv692426, nssv683688, nssv676861, nssv651821, nssv656885, nssv665585, nssv687403, nssv684828, nssv652869, nssv702402
Samples
Known GenesZNF444, ZNF787
MethodSNP array
AnalysisSample-level CNVs
PlatformGPL6434
Comments
ReferenceShaikh_et_al_2009
Pubmed ID19592680
Accession Number(s)nsv517365
Frequency
Sample Size2026
Observed Gain0
Observed Loss16
Observed Complex0
Frequencyn/a


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