A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5456391



Internal ID234460
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr6:37073236..37077555hg38UCSC Ensembl
chr6:37041012..37045331hg19UCSC Ensembl
Cytoband6p21.2
Allele length
AssemblyAllele length
hg384320
hg194320
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv16982108
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceByrska_Bishop_et_al_2022
Pubmed ID36055201
Accession Number(s)nsv5456391
Frequency
Sample Size3202
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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