A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv524476



Internal ID15105083
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr15:41397034..41528002hg38UCSC Ensembl
Innerchr15:41689232..41820200hg19UCSC Ensembl
Innerchr15:39476524..39607492hg18UCSC Ensembl
Innerchr15:39476524..39607492hg17UCSC Ensembl
Cytoband15q15.1
Allele length
AssemblyAllele length
hg38130969
hg19130969
hg18130969
hg17130969
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv700414
Samples
Known GenesITPKA, LTK, NDUFAF1, RPAP1, RTF1
MethodSNP array
AnalysisSample-level CNVs
PlatformGPL6434
Comments
ReferenceShaikh_et_al_2009
Pubmed ID19592680
Accession Number(s)nsv524476
Frequency
Sample Size2026
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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