A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6437234



Internal ID21094787
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr11:6602704..6989609hg38UCSC Ensembl
chr11:6623934..7010840hg19UCSC Ensembl
Cytoband11p15.4
Allele length
AssemblyAllele length
hg38386906
hg19386907
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18180630
Samples
Known GenesDCHS1, GVINP1, ILK, MRPL17, OR10A2, OR10A4, OR10A5, OR2AG1, OR2AG2, OR2D2, OR2D3, OR6A2, RRP8, TAF10, TPP1, ZNF215
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6437234
Frequency
Sample Size19652
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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