A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv518513



Internal ID15099120
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr15:36973546..36984038hg38UCSC Ensembl
Innerchr15:37265747..37276239hg19UCSC Ensembl
Innerchr15:35053039..35063531hg18UCSC Ensembl
Innerchr15:35053039..35063531hg17UCSC Ensembl
Cytoband15q14
Allele length
AssemblyAllele length
hg3810493
hg1910493
hg1810493
hg1710493
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv695953
Samples
Known GenesMEIS2
MethodSNP array
AnalysisSample-level CNVs
PlatformGPL6434
Comments
ReferenceShaikh_et_al_2009
Pubmed ID19592680
Accession Number(s)nsv518513
Frequency
Sample Size2026
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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