A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv569699



Internal ID16357108
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr15:63190006..63191003hg38UCSC Ensembl
Innerchr15:63482205..63483202hg19UCSC Ensembl
Innerchr15:61269258..61270255hg18UCSC Ensembl
Cytoband15q22.2
Allele length
AssemblyAllele length
hg38998
hg19998
hg18998
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv4571n54
Supporting Variantsnssv843966
Samples
Known GenesRAB8B
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)nsv569699
Frequency
Sample Size17421
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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