A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv664281



Internal ID15054247
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr15:90868426..90981967hg38UCSC Ensembl
Innerchr15:91411656..91525197hg19UCSC Ensembl
Innerchr15:89212660..89326201hg18UCSC Ensembl
Innerchr15:89212660..89326201hg17UCSC Ensembl
Cytoband15q26.1
Allele length
AssemblyAllele length
hg38113542
hg19113542
hg18113542
hg17113542
Variant TypeCNV loss
Copy Number
Allele StateHeterozygous
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv515661
Supporting Variants
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)nssv664281
Frequency
Sample Size2026
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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