A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv516488



Internal ID15443781
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr15:66203916..66207548hg38UCSC Ensembl
Innerchr15:66496254..66499886hg19UCSC Ensembl
Innerchr15:64283308..64286940hg18UCSC Ensembl
Innerchr15:64283308..64286940hg17UCSC Ensembl
Cytoband15q22.31
Allele length
AssemblyAllele length
hg383633
hg193633
hg183633
hg173633
Variant TypeCNV gain+loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv668669, nssv696931, nssv674632
Samples
Known GenesMEGF11
MethodSNP array
AnalysisSample-level CNVs
PlatformGPL6434
Comments
ReferenceShaikh_et_al_2009
Pubmed ID19592680
Accession Number(s)nsv516488
Frequency
Sample Size2026
Observed Gain2
Observed Loss1
Observed Complex0
Frequencyn/a


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