A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv528361



Internal ID15108968
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr19:56127476..56177201hg38UCSC Ensembl
Innerchr19:56638845..56688570hg19UCSC Ensembl
Innerchr19:61330657..61380382hg18UCSC Ensembl
Innerchr19:61330657..61380382hg17UCSC Ensembl
Cytoband19q13.42
Allele length
AssemblyAllele length
hg3849726
hg1949726
hg1849726
hg1749726
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv704948
Samples
Known GenesGALP, ZNF444
MethodSNP array
AnalysisSample-level CNVs
PlatformGPL6434
Comments
ReferenceShaikh_et_al_2009
Pubmed ID19592680
Accession Number(s)nsv528361
Frequency
Sample Size2026
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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