A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv570823



Internal ID16358232
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr15:100879516..100880220hg38UCSC Ensembl
Innerchr15:101419721..101420425hg19UCSC Ensembl
Innerchr15:99237244..99237948hg18UCSC Ensembl
Cytoband15q26.3
Allele length
AssemblyAllele length
hg38705
hg19705
hg18705
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv4787n54
Supporting Variantsnssv851014, nssv851013
Samples
Known GenesALDH1A3
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)nsv570823
Frequency
Sample Size17421
Observed Gain0
Observed Loss2
Observed Complex0
Frequencyn/a


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