A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5454898



Internal ID232992
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr6:123010102..123168051hg38UCSC Ensembl
chr6:123331247..123489196hg19UCSC Ensembl
Cytoband6q22.31
Allele length
AssemblyAllele length
hg38157950
hg19157950
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv16969895
Samples
Known GenesCLVS2
MethodSequencing
Analysis
Platform
Comments
ReferenceByrska_Bishop_et_al_2022
Pubmed ID36055201
Accession Number(s)nsv5454898
Frequency
Sample Size3202
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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