A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv570353



Internal ID16357762
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr15:85753010..85760520hg38UCSC Ensembl
Innerchr15:86296241..86303751hg19UCSC Ensembl
Innerchr15:84097245..84104755hg18UCSC Ensembl
Cytoband15q25.3
Allele length
AssemblyAllele length
hg387511
hg197511
hg187511
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv848128
Samples
Known GenesKLHL25
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)nsv570353
Frequency
Sample Size17421
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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