A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6145238



Internal ID344443
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr16:10000..15925hg38UCSC Ensembl
chr16:60001..65925hg19UCSC Ensembl
Cytoband16p13.3
Allele length
AssemblyAllele length
hg385926
hg195925
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17705624
Samples
Known GenesDDX11L10
MethodSequencing
Analysis
Platform
Comments
ReferenceByrska_Bishop_et_al_2022
Pubmed ID36055201
Accession Number(s)nsv6145238
Frequency
Sample Size3202
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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