A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1040955



Internal ID19130174
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr15:66946476..66969175hg38UCSC Ensembl
Innerchr15:67238814..67261513hg19UCSC Ensembl
Innerchr15:65025868..65048567hg18UCSC Ensembl
Cytoband15q22.32
Allele length
AssemblyAllele length
hg3822700
hg1922700
hg1822700
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv3553649
Samples
Known Genes
MethodSNP array
AnalysisAffymetrix SNP array copy number analysis
PlatformAffymetrix SNP Array 6.0
Comments
ReferenceCoe_et_al_2014
Pubmed ID25217958
Accession Number(s)nsv1040955
Frequency
Sample Size11257
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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