A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5458897



Internal ID236917
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr6:36102343..36102416hg38UCSC Ensembl
chr6:36070120..36070193hg19UCSC Ensembl
Cytoband6p21.31
Allele length
AssemblyAllele length
hg3874
hg1974
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv16981301
Samples
Known GenesMAPK14
MethodSequencing
Analysis
Platform
Comments
ReferenceByrska_Bishop_et_al_2022
Pubmed ID36055201
Accession Number(s)nsv5458897
Frequency
Sample Size3202
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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