A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1019336



Internal ID19108554
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr6:61119045..61350771hg38UCSC Ensembl
Innerchr6:61886428..62118671hg19UCSC Ensembl
Innerchr6:61944387..62176630hg18UCSC Ensembl
Cytoband6q11.1
Allele length
AssemblyAllele length
hg38231727
hg19232244
hg18232244
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv5984n100
Supporting Variantsnssv3657581
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)nsv1019336
Frequency
Sample Size11257
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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