A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv525461



Internal ID15452754
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr15:42770350..43189929hg38UCSC Ensembl
Innerchr15:43062548..43482127hg19UCSC Ensembl
Innerchr15:40849840..41269419hg18UCSC Ensembl
Innerchr15:40849840..41269419hg17UCSC Ensembl
Cytoband15q15.2
Allele length
AssemblyAllele length
hg38419580
hg19419580
hg18419580
hg17419580
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv701589
Samples
Known GenesCCNDBP1, TMEM62, TTBK2, UBR1
MethodSNP array
AnalysisSample-level CNVs
PlatformGPL6434
Comments
ReferenceShaikh_et_al_2009
Pubmed ID19592680
Accession Number(s)nsv525461
Frequency
Sample Size2026
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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