A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1045058



Internal ID19134277
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr15:81703904..81804141hg38UCSC Ensembl
Innerchr15:81996245..82096482hg19UCSC Ensembl
Innerchr15:79783300..79883537hg18UCSC Ensembl
Cytoband15q25.2
Allele length
AssemblyAllele length
hg38100238
hg19100238
hg18100238
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv2635n100
Supporting Variantsnssv3718101, nssv3554611
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)nsv1045058
Frequency
Sample Size11257
Observed Gain2
Observed Loss0
Observed Complex0
Frequencyn/a


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