A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1016779



Internal ID19105996
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr5:6154192..6189668hg38UCSC Ensembl
Innerchr5:6154305..6189781hg19UCSC Ensembl
Innerchr5:6207305..6242781hg18UCSC Ensembl
Cytoband5p15.31
Allele length
AssemblyAllele length
hg3835477
hg1935477
hg1835477
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv5558n100
Supporting Variantsnssv3638599
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)nsv1016779
Frequency
Sample Size11257
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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