A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv570828



Internal ID16011551
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr15:101086688..101408007hg38UCSC Ensembl
Innerchr15:101626893..101948212hg19UCSC Ensembl
Innerchr15:99444416..99765735hg18UCSC Ensembl
Cytoband15q26.3
Allele length
AssemblyAllele length
hg38321320
hg19321320
hg18321320
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv851018
Samples
Known GenesCHSY1, LOC100507472, PCSK6, SNRPA1, VIMP
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)nsv570828
Frequency
Sample Size17421
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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