A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1022196



Internal ID19111414
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr5:15520..49809hg38UCSC Ensembl
Innerchr5:15520..49924hg19UCSC Ensembl
Innerchr5:68520..102924hg18UCSC Ensembl
Cytoband5p15.33
Allele length
AssemblyAllele length
hg3834290
hg1934405
hg1834405
Variant TypeCNV gain+loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv5510n100
Supporting Variantsnssv3636495, nssv3636494, nssv3636496
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)nsv1022196
Frequency
Sample Size11257
Observed Gain2
Observed Loss1
Observed Complex0
Frequencyn/a


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