A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv850964



Internal ID16144920
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr15:100879147..100879954hg38UCSC Ensembl
Innerchr15:101419352..101420159hg19UCSC Ensembl
Innerchr15:99236875..99237682hg18UCSC Ensembl
Cytoband15q26.3
Allele length
AssemblyAllele length
hg38808
hg19808
hg18808
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv570808
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)nssv850964
Frequency
Sample Size17421
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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