A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv515853



Internal ID15442910
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr3:16197487..16199569hg38UCSC Ensembl
Innerchr3:16238994..16241076hg19UCSC Ensembl
Innerchr3:16213998..16216080hg18UCSC Ensembl
Innerchr3:16213998..16216080hg17UCSC Ensembl
Cytoband3p24.3
Allele length
AssemblyAllele length
hg382083
hg192083
hg182083
hg172083
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv665017, nssv681223
Samples
Known GenesGALNT15
MethodSNP array
AnalysisSample-level CNVs
PlatformGPL6434
Comments
ReferenceShaikh_et_al_2009
Pubmed ID19592680
Accession Number(s)nsv515853
Frequency
Sample Size2026
Observed Gain0
Observed Loss2
Observed Complex0
Frequencyn/a


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