A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv518441



Internal ID15099048
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr19:11717595..11728780hg38UCSC Ensembl
Innerchr19:11828410..11839595hg19UCSC Ensembl
Innerchr19:11689410..11700595hg18UCSC Ensembl
Innerchr19:11689410..11700595hg17UCSC Ensembl
Cytoband19p13.2
Allele length
AssemblyAllele length
hg3811186
hg1911186
hg1811186
hg1711186
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv695878
Samples
Known GenesZNF823
MethodSNP array
AnalysisSample-level CNVs
PlatformGPL6434
Comments
ReferenceShaikh_et_al_2009
Pubmed ID19592680
Accession Number(s)nsv518441
Frequency
Sample Size2026
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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