A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6144455



Internal ID343660
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr14:105589238..105858290hg38UCSC Ensembl
chr14:106055575..106324459hg19UCSC Ensembl
Cytoband14q32.33
Allele length
AssemblyAllele length
hg38269053
hg19268885
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17700624
Samples
Known GenesELK2AP, MIR8071-1, MIR8071-2
MethodSequencing
Analysis
Platform
Comments
ReferenceByrska_Bishop_et_al_2022
Pubmed ID36055201
Accession Number(s)nsv6144455
Frequency
Sample Size3202
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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