A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6439692



Internal ID21097245
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr11:4682156..5202827hg38UCSC Ensembl
chr11:4703386..5224057hg19UCSC Ensembl
Cytoband11p15.4
Allele length
AssemblyAllele length
hg38520672
hg19520672
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv958n223
Supporting Variantsnssv18188514
Samples
Known GenesMMP26, OR51A2, OR51A4, OR51A7, OR51E2, OR51F1, OR51F2, OR51G1, OR51G2, OR51L1, OR51S1, OR51T1, OR51V1, OR52A1, OR52A5, OR52E2, OR52J3, OR52R1
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6439692
Frequency
Sample Size19652
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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