A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv850952



Internal ID15798222
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr15:100878753..100880008hg38UCSC Ensembl
Innerchr15:101418958..101420213hg19UCSC Ensembl
Innerchr15:99236481..99237736hg18UCSC Ensembl
Cytoband15q26.3
Allele length
AssemblyAllele length
hg381256
hg191256
hg181256
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv570804
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)nssv850952
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