A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1045907



Internal ID19135126
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr15:62146508..62169066hg38UCSC Ensembl
Innerchr15:62438707..62461265hg19UCSC Ensembl
Innerchr15:60225999..60248557hg18UCSC Ensembl
Cytoband15q22.2
Allele length
AssemblyAllele length
hg3822559
hg1922559
hg1822559
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv3553637, nssv3553638, nssv3553636, nssv3553639
Samples
Known GenesC2CD4B
MethodSNP array
AnalysisAffymetrix SNP array copy number analysis
PlatformAffymetrix SNP Array 6.0
Comments
ReferenceCoe_et_al_2014
Pubmed ID25217958
Accession Number(s)nsv1045907
Frequency
Sample Size11257
Observed Gain4
Observed Loss0
Observed Complex0
Frequencyn/a


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