A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv515661



Internal ID15096268
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr15:90866779..90981967hg38UCSC Ensembl
Innerchr15:91410009..91525197hg19UCSC Ensembl
Innerchr15:89211013..89326201hg18UCSC Ensembl
Innerchr15:89211013..89326201hg17UCSC Ensembl
Cytoband15q26.1
Allele length
AssemblyAllele length
hg38115189
hg19115189
hg18115189
hg17115189
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv665011, nssv664281, nssv679616
Samples
Known GenesFES, FURIN, HDDC3, MAN2A2, PRC1, PRC1-AS1, RCCD1, UNC45A
MethodSNP array
AnalysisSample-level CNVs
PlatformGPL6434
Comments
ReferenceShaikh_et_al_2009
Pubmed ID19592680
Accession Number(s)nsv515661
Frequency
Sample Size2026
Observed Gain0
Observed Loss3
Observed Complex0
Frequencyn/a


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