A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv525611



Internal ID15106218
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr19:57957788..57959153hg38UCSC Ensembl
Innerchr19:58469156..58470521hg19UCSC Ensembl
Innerchr19:63160968..63162333hg18UCSC Ensembl
Innerchr19:63160968..63162333hg17UCSC Ensembl
Cytoband19q13.43
Allele length
AssemblyAllele length
hg381366
hg191366
hg181366
hg171366
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv701756
Samples
Known GenesC19orf18
MethodSNP array
AnalysisSample-level CNVs
PlatformGPL6434
Comments
ReferenceShaikh_et_al_2009
Pubmed ID19592680
Accession Number(s)nsv525611
Frequency
Sample Size2026
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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