A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv521299



Internal ID15448592
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr15:43622175..43647444hg38UCSC Ensembl
Innerchr15:43914373..43939642hg19UCSC Ensembl
Innerchr15:41701665..41726934hg18UCSC Ensembl
Innerchr15:41701665..41726934hg17UCSC Ensembl
Cytoband15q15.3
Allele length
AssemblyAllele length
hg3825270
hg1925270
hg1825270
hg1725270
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv146n21
Supporting Variantsnssv697906
Samples
Known GenesCATSPER2
MethodSNP array
AnalysisSample-level CNVs
PlatformGPL6434
Comments
ReferenceShaikh_et_al_2009
Pubmed ID19592680
Accession Number(s)nsv521299
Frequency
Sample Size2026
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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