A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1026520



Internal ID19115738
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr5:110869856..110908551hg38UCSC Ensembl
Innerchr5:110205555..110244250hg19UCSC Ensembl
Innerchr5:110233454..110272149hg18UCSC Ensembl
Cytoband5q22.1
Allele length
AssemblyAllele length
hg3838696
hg1938696
hg1838696
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv3647024
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)nsv1026520
Frequency
Sample Size11257
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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