A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv4734020



Internal ID20509953
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr6:149759082..149759701hg38UCSC Ensembl
chr6:150080218..150080837hg19UCSC Ensembl
Cytoband6q25.1
Allele length
AssemblyAllele length
hg38620
hg19620
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv16265434
Samples
Known GenesPCMT1
MethodSequencing
Analysis
Platform
Comments
ReferenceQuan_et_al_2021
Pubmed ID34034800
Accession Number(s)nsv4734020
Frequency
Sample Size25
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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