A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1022531



Internal ID19111749
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr5:15520..99326hg38UCSC Ensembl
Innerchr5:15520..99441hg19UCSC Ensembl
Innerchr5:68520..152441hg18UCSC Ensembl
Cytoband5p15.33
Allele length
AssemblyAllele length
hg3883807
hg1983922
hg1883922
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv5513n100
Supporting Variantsnssv3636521, nssv3636522
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)nsv1022531
Frequency
Sample Size11257
Observed Gain2
Observed Loss0
Observed Complex0
Frequencyn/a


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