A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv3169377



Internal ID21313860
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr15:65874660..65940586hg38UCSC Ensembl
Outerchr15:65870434..65946706hg38UCSC Ensembl
Innerchr15:66166998..66232924hg19UCSC Ensembl
Outerchr15:66162772..66239044hg19UCSC Ensembl
Innerchr15:63954052..64019978hg18UCSC Ensembl
Outerchr15:63949826..64026098hg18UCSC Ensembl
Cytoband15q22.31
Allele length
AssemblyAllele length
hg3876273
hg1976273
hg1876273
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv14249422
SamplesNGO_25
Known GenesMEGF11, RAB11A
MethodSNP array
Analysis
PlatformAffymetrix Genome-wide SNP array 6.0
Comments
ReferenceFu_et_al_2018
Pubmed ID29476164
Accession Number(s)nsv3169377
Frequency
Sample Size93
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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