A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1026273



Internal ID18768805
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr5:15520..115984hg38UCSC Ensembl
Innerchr5:15520..116099hg19UCSC Ensembl
Innerchr5:68520..169099hg18UCSC Ensembl
Cytoband5p15.33
Allele length
AssemblyAllele length
hg38100465
hg19100580
hg18100580
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv5514n100
Supporting Variantsnssv3636525
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)nsv1026273
Frequency
Sample Size29084
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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