A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv569410



Internal ID16356819
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr15:51965677..51980935hg38UCSC Ensembl
Innerchr15:52257874..52273132hg19UCSC Ensembl
Innerchr15:50045166..50060424hg18UCSC Ensembl
Cytoband15q21.2
Allele length
AssemblyAllele length
hg3815259
hg1915259
hg1815259
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv842984
Samples
Known GenesLEO1
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)nsv569410
Frequency
Sample Size17421
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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