A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv515534



Internal ID15443145
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr15:52706065..52733495hg38UCSC Ensembl
Innerchr15:52998262..53025692hg19UCSC Ensembl
Innerchr15:50785554..50812984hg18UCSC Ensembl
Innerchr15:50785554..50812984hg17UCSC Ensembl
Cytoband15q21.2
Allele length
AssemblyAllele length
hg3827431
hg1927431
hg1827431
hg1727431
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv673845, nssv663850
Samples
Known Genes
MethodSNP array
AnalysisSample-level CNVs
PlatformGPL6434
Comments
ReferenceShaikh_et_al_2009
Pubmed ID19592680
Accession Number(s)nsv515534
Frequency
Sample Size2026
Observed Gain2
Observed Loss0
Observed Complex0
Frequencyn/a


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