A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv570816



Internal ID16011539
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr15:100879313..100881468hg38UCSC Ensembl
Innerchr15:101419518..101421673hg19UCSC Ensembl
Innerchr15:99237041..99239196hg18UCSC Ensembl
Cytoband15q26.3
Allele length
AssemblyAllele length
hg382156
hg192156
hg182156
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv851002
Samples
Known GenesALDH1A3
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)nsv570816
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