A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv16263148



Internal ID20472366
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr20:41555233..41555362hg38UCSC Ensembl
chr20:40183872..40184001hg19UCSC Ensembl
Cytoband20q12
Allele length
AssemblyAllele length
hg38130
hg19130
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv4732193
Supporting Variants
Samples
Known GenesCHD6
MethodSequencing
Analysis
Platform
Comments
ReferenceQuan_et_al_2021
Pubmed ID34034800
Accession Number(s)nssv16263148
Frequency
Sample Size25
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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