A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv570807



Internal ID16358216
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr15:100879147..100879851hg38UCSC Ensembl
Innerchr15:101419352..101420056hg19UCSC Ensembl
Innerchr15:99236875..99237579hg18UCSC Ensembl
Cytoband15q26.3
Allele length
AssemblyAllele length
hg38705
hg19705
hg18705
Variant TypeCNV gain+loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv4782n54
Supporting Variantsnssv850961, nssv850959, nssv850958, nssv850960
Samples
Known GenesALDH1A3
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)nsv570807
Frequency
Sample Size17421
Observed Gain1
Observed Loss3
Observed Complex0
Frequencyn/a


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