A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1055090



Internal ID18797621
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr15:66217529..66298669hg38UCSC Ensembl
Innerchr15:66509867..66591007hg19UCSC Ensembl
Innerchr15:64296921..64378061hg18UCSC Ensembl
Cytoband15q22.31
Allele length
AssemblyAllele length
hg3881141
hg1981141
hg1881141
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv3717954
Samples
Known GenesDIS3L, MEGF11
MethodSNP array
AnalysisAffymetrix SNP array copy number analysis
PlatformAffymetrix SNP Array 6.0
Comments
ReferenceCoe_et_al_2014
Pubmed ID25217958
Accession Number(s)nsv1055090
Frequency
Sample Size29084
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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