A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv521742



Internal ID15449035
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr15:71428605..71438816hg38UCSC Ensembl
Innerchr15:71720944..71731155hg19UCSC Ensembl
Innerchr15:69507998..69518209hg18UCSC Ensembl
Innerchr15:69507998..69518209hg17UCSC Ensembl
Cytoband15q23
Allele length
AssemblyAllele length
hg3810212
hg1910212
hg1810212
hg1710212
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv694506
Samples
Known GenesTHSD4
MethodSNP array
AnalysisSample-level CNVs
PlatformGPL6434
Comments
ReferenceShaikh_et_al_2009
Pubmed ID19592680
Accession Number(s)nsv521742
Frequency
Sample Size2026
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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