A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1053391



Internal ID19142610
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr15:60966393..61071078hg38UCSC Ensembl
Innerchr15:61258592..61363277hg19UCSC Ensembl
Innerchr15:59045884..59150569hg18UCSC Ensembl
Cytoband15q22.2
Allele length
AssemblyAllele length
hg38104686
hg19104686
hg18104686
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv2612n100
Supporting Variantsnssv3553627
Samples
Known GenesRORA
MethodSNP array
AnalysisAffymetrix SNP array copy number analysis
PlatformAffymetrix SNP Array 6.0
Comments
ReferenceCoe_et_al_2014
Pubmed ID25217958
Accession Number(s)nsv1053391
Frequency
Sample Size11257
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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