A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1022336



Internal ID19111554
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr6:5144960..5200453hg38UCSC Ensembl
Innerchr6:5145194..5200687hg19UCSC Ensembl
Innerchr6:5090193..5145686hg18UCSC Ensembl
Cytoband6p25.1
Allele length
AssemblyAllele length
hg3855494
hg1955494
hg1855494
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv5913n100
Supporting Variantsnssv3654737
Samples
Known GenesLYRM4, MIR3691
MethodSNP array
AnalysisAffymetrix SNP array copy number analysis
PlatformAffymetrix SNP Array 6.0
Comments
ReferenceCoe_et_al_2014
Pubmed ID25217958
Accession Number(s)nsv1022336
Frequency
Sample Size11257
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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