A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv16265434



Internal ID20474652
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 StatusS
Merged Variantsnsv4734020
Supporting Variants
Samples
Known GenesPCMT1
MethodSequencing
Analysis
Platform
Comments
ReferenceQuan_et_al_2021
Pubmed ID34034800
Accession Number(s)nssv16265434
Frequency
Sample Size25
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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