A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv525114



Internal ID8419389
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr15:88853826..88855374hg38UCSC Ensembl
Innerchr15:89397057..89398605hg19UCSC Ensembl
Innerchr15:87198061..87199609hg18UCSC Ensembl
Innerchr15:87198061..87199609hg17UCSC Ensembl
Cytoband15q26.1
Allele length
AssemblyAllele length
hg381549
hg191549
hg181549
hg171549
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv701178
Samples
Known GenesACAN
MethodSNP array
AnalysisSample-level CNVs
PlatformGPL6434
Comments
ReferenceShaikh_et_al_2009
Pubmed ID19592680
Accession Number(s)nsv525114
Frequency
Sample Size2026
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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