A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv16262874



Internal ID20472092
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr4:76775895..76776197hg38UCSC Ensembl
chr4:77697048..77697350hg19UCSC Ensembl
Cytoband4q21.1
Allele length
AssemblyAllele length
hg38303
hg19303
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv4734995
Supporting Variants
Samples
Known GenesSHROOM3
MethodSequencing
Analysis
Platform
Comments
ReferenceQuan_et_al_2021
Pubmed ID34034800
Accession Number(s)nssv16262874
Frequency
Sample Size25
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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