A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5464025



Internal ID241912
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr6:54233952..54259135hg38UCSC Ensembl
chr6:54098750..54123933hg19UCSC Ensembl
Cytoband6p12.1
Allele length
AssemblyAllele length
hg3825184
hg1925184
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv16983318
Samples
Known GenesMLIP
MethodSequencing
Analysis
Platform
Comments
ReferenceByrska_Bishop_et_al_2022
Pubmed ID36055201
Accession Number(s)nsv5464025
Frequency
Sample Size3202
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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