A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv516532



Internal ID15097139
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr15:89389564..89405705hg38UCSC Ensembl
Innerchr15:89932795..89948936hg19UCSC Ensembl
Innerchr15:87733799..87749940hg18UCSC Ensembl
Innerchr15:87733799..87749940hg17UCSC Ensembl
Cytoband15q26.1
Allele length
AssemblyAllele length
hg3816142
hg1916142
hg1816142
hg1716142
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv659355, nssv668920, nssv669595, nssv688004
Samples
Known GenesLINC00925
MethodSNP array
AnalysisSample-level CNVs
PlatformGPL6434
Comments
ReferenceShaikh_et_al_2009
Pubmed ID19592680
Accession Number(s)nsv516532
Frequency
Sample Size2026
Observed Gain0
Observed Loss4
Observed Complex0
Frequencyn/a


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