A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv522659



Internal ID15103266
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr19:11708378..11721468hg38UCSC Ensembl
Innerchr19:11819193..11832283hg19UCSC Ensembl
Innerchr19:11680193..11693283hg18UCSC Ensembl
Innerchr19:11680193..11693283hg17UCSC Ensembl
Cytoband19p13.2
Allele length
AssemblyAllele length
hg3813091
hg1913091
hg1813091
hg1713091
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv706061
Samples
Known GenesZNF823
MethodSNP array
AnalysisSample-level CNVs
PlatformGPL6434
Comments
ReferenceShaikh_et_al_2009
Pubmed ID19592680
Accession Number(s)nsv522659
Frequency
Sample Size2026
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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