A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv569803



Internal ID16010526
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr15:67585107..68124237hg38UCSC Ensembl
Innerchr15:67877445..68416575hg19UCSC Ensembl
Innerchr15:65664499..66203629hg18UCSC Ensembl
Cytoband15q23
Allele length
AssemblyAllele length
hg38539131
hg19539131
hg18539131
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv844363
Samples
Known GenesMAP2K5, PIAS1, SKOR1
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)nsv569803
Frequency
Sample Size17421
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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