A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv570579



Internal ID16357988
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr15:96112159..96133300hg38UCSC Ensembl
Innerchr15:96655388..96676529hg19UCSC Ensembl
Innerchr15:94456392..94477533hg18UCSC Ensembl
Cytoband15q26.2
Allele length
AssemblyAllele length
hg3821142
hg1921142
hg1821142
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv849101
Samples
Known Genes
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)nsv570579
Frequency
Sample Size17421
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


Hosted by The Centre for Applied Genomics
Grant support for DGV
Please read the usage disclaimer