A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv4737176



Internal ID20513134
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 StatusM
Merged Variants
Supporting Variantsnssv16263856
Samples
Known GenesATP13A4
MethodSequencing
Analysis
Platform
Comments
ReferenceQuan_et_al_2021
Pubmed ID34034800
Accession Number(s)nsv4737176
Frequency
Sample Size25
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


Hosted by The Centre for Applied Genomics
Grant support for DGV
Please read the usage disclaimer