A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv570386



Internal ID16011109
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr15:89464359..89517327hg38UCSC Ensembl
Innerchr15:90007590..90060558hg19UCSC Ensembl
Innerchr15:87808594..87861562hg18UCSC Ensembl
Cytoband15q26.1
Allele length
AssemblyAllele length
hg3852969
hg1952969
hg1852969
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv1149604
SamplesHGDP00888
Known GenesLINC00928, RHCG
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)nsv570386
Frequency
Sample Size17421
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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