A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5457897



Internal ID235932
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr6:124745949..124746082hg38UCSC Ensembl
chr6:125067095..125067228hg19UCSC Ensembl
Cytoband6q22.31
Allele length
AssemblyAllele length
hg38134
hg19134
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv16969016
Samples
Known GenesNKAIN2
MethodSequencing
Analysis
Platform
Comments
ReferenceByrska_Bishop_et_al_2022
Pubmed ID36055201
Accession Number(s)nsv5457897
Frequency
Sample Size3202
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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