A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv570831



Internal ID16358240
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr15:101166509..101175315hg38UCSC Ensembl
Innerchr15:101706714..101715520hg19UCSC Ensembl
Innerchr15:99524237..99533043hg18UCSC Ensembl
Cytoband15q26.3
Allele length
AssemblyAllele length
hg388807
hg198807
hg188807
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv4788n54
Supporting Variantsnssv851022, nssv851023, nssv851021
Samples
Known Genes
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)nsv570831
Frequency
Sample Size17421
Observed Gain0
Observed Loss3
Observed Complex0
Frequencyn/a


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