A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1020918



Internal ID19110136
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr6:149649..204011hg38UCSC Ensembl
Innerchr6:149649..204011hg19UCSC Ensembl
Innerchr6:94649..149011hg18UCSC Ensembl
Cytoband6p25.3
Allele length
AssemblyAllele length
hg3854363
hg1954363
hg1854363
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv5865n100
Supporting Variantsnssv3650362
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)nsv1020918
Frequency
Sample Size11257
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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