A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv16279432



Internal ID20488650
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr8:122875130..122875181hg38UCSC Ensembl
chr8:123887369..123887420hg19UCSC Ensembl
Cytoband8q24.13
Allele length
AssemblyAllele length
hg3852
hg1952
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv4739917
Supporting Variants
Samples
Known GenesZHX2
MethodSequencing
Analysis
Platform
Comments
ReferenceQuan_et_al_2021
Pubmed ID34034800
Accession Number(s)nssv16279432
Frequency
Sample Size25
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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