A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv520539



Internal ID15447832
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr15:60999230..61009847hg38UCSC Ensembl
Innerchr15:61291429..61302046hg19UCSC Ensembl
Innerchr15:59078721..59089338hg18UCSC Ensembl
Innerchr15:59078721..59089338hg17UCSC Ensembl
Cytoband15q22.2
Allele length
AssemblyAllele length
hg3810618
hg1910618
hg1810618
hg1710618
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv697475
Samples
Known GenesRORA
MethodSNP array
AnalysisSample-level CNVs
PlatformGPL6434
Comments
ReferenceShaikh_et_al_2009
Pubmed ID19592680
Accession Number(s)nsv520539
Frequency
Sample Size2026
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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