A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv518075



Internal ID15445368
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr19:4933216..4945962hg38UCSC Ensembl
Innerchr19:4933228..4945974hg19UCSC Ensembl
Innerchr19:4884228..4896974hg18UCSC Ensembl
Innerchr19:4884228..4896974hg17UCSC Ensembl
Cytoband19p13.3
Allele length
AssemblyAllele length
hg3812747
hg1912747
hg1812747
hg1712747
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv694198
Samples
Known GenesUHRF1
MethodSNP array
AnalysisSample-level CNVs
PlatformGPL6434
Comments
ReferenceShaikh_et_al_2009
Pubmed ID19592680
Accession Number(s)nsv518075
Frequency
Sample Size2026
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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