A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv16272046



Internal ID20481264
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr8:105533810..105533923hg38UCSC Ensembl
chr8:106546038..106546151hg19UCSC Ensembl
Cytoband8q23.1
Allele length
AssemblyAllele length
hg38114
hg19114
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv4735539
Supporting Variants
Samples
Known GenesZFPM2
MethodSequencing
Analysis
Platform
Comments
ReferenceQuan_et_al_2021
Pubmed ID34034800
Accession Number(s)nssv16272046
Frequency
Sample Size25
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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