A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1017060



Internal ID19106277
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr5:18607196..18662987hg38UCSC Ensembl
Innerchr5:18607305..18663096hg19UCSC Ensembl
Innerchr5:18643062..18698853hg18UCSC Ensembl
Cytoband5p14.3
Allele length
AssemblyAllele length
hg3855792
hg1955792
hg1855792
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv5593n100
Supporting Variantsnssv3635866, nssv3635865, nssv3635864
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)nsv1017060
Frequency
Sample Size11257
Observed Gain3
Observed Loss0
Observed Complex0
Frequencyn/a


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