A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5461753



Internal ID239699
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr6:21163889..21164558hg38UCSC Ensembl
chr6:21164120..21164789hg19UCSC Ensembl
Cytoband6p22.3
Allele length
AssemblyAllele length
hg38670
hg19670
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv16982204
Samples
Known GenesCDKAL1
MethodSequencing
Analysis
Platform
Comments
ReferenceByrska_Bishop_et_al_2022
Pubmed ID36055201
Accession Number(s)nsv5461753
Frequency
Sample Size3202
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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