A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv16263856



Internal ID20473074
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr3:193514434..193514673hg38UCSC Ensembl
chr3:193232223..193232462hg19UCSC Ensembl
Cytoband3q29
Allele length
AssemblyAllele length
hg38240
hg19240
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv4737176
Supporting Variants
Samples
Known GenesATP13A4
MethodSequencing
Analysis
Platform
Comments
ReferenceQuan_et_al_2021
Pubmed ID34034800
Accession Number(s)nssv16263856
Frequency
Sample Size25
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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