A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1054037



Internal ID19143256
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr13:61484203..61520642hg38UCSC Ensembl
Innerchr13:62058336..62094775hg19UCSC Ensembl
Innerchr13:60956337..60992776hg18UCSC Ensembl
Cytoband13q21.2
Allele length
AssemblyAllele length
hg3836440
hg1936440
hg1836440
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv3526589
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)nsv1054037
Frequency
Sample Size11257
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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