A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1047176



Internal ID18789707
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr15:66036143..66310781hg38UCSC Ensembl
Innerchr15:66328481..66603119hg19UCSC Ensembl
Innerchr15:64115535..64390173hg18UCSC Ensembl
Cytoband15q22.31
Allele length
AssemblyAllele length
hg38274639
hg19274639
hg18274639
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv3553647
Samples
Known GenesDIS3L, MEGF11, MIR4311
MethodSNP array
AnalysisAffymetrix SNP array copy number analysis
PlatformAffymetrix SNP Array 6.0
Comments
ReferenceCoe_et_al_2014
Pubmed ID25217958
Accession Number(s)nsv1047176
Frequency
Sample Size29084
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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