A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv850995



Internal ID15798265
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr15:100879313..100880164hg38UCSC Ensembl
Innerchr15:101419518..101420369hg19UCSC Ensembl
Innerchr15:99237041..99237892hg18UCSC Ensembl
Cytoband15q26.3
Allele length
AssemblyAllele length
hg38852
hg19852
hg18852
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv570813
Supporting Variants
Samples
Known GenesALDH1A3
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)nssv850995
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