A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv570813



Internal ID16011536
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 gain+loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv4783n54
Supporting Variantsnssv850994, nssv850995, nssv850993, nssv850992
Samples
Known GenesALDH1A3
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)nsv570813
Frequency
Sample Size17421
Observed Gain2
Observed Loss2
Observed Complex0
Frequencyn/a


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