A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv674632



Internal ID15411284
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
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv516488
Supporting Variants
Samples
Known GenesMEGF11
MethodSNP array
AnalysisSample-level CNVs
PlatformGPL6434
Comments
ReferenceShaikh_et_al_2009
Pubmed ID19592680
Accession Number(s)nssv674632
Frequency
Sample Size2026
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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