A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5456527



Internal ID234591
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr6:21716194..21720966hg38UCSC Ensembl
chr6:21716425..21721197hg19UCSC Ensembl
Cytoband6p22.3
Allele length
AssemblyAllele length
hg384773
hg194773
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv16982246
Samples
Known GenesCASC15
MethodSequencing
Analysis
Platform
Comments
ReferenceByrska_Bishop_et_al_2022
Pubmed ID36055201
Accession Number(s)nsv5456527
Frequency
Sample Size3202
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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