A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv4749746



Internal ID20525779
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr3:195412946..195423719hg38UCSC Ensembl
chr3:195133675..195144448hg19UCSC Ensembl
Cytoband3q29
Allele length
AssemblyAllele length
hg3810774
hg1910774
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv16295855
Samples
Known GenesACAP2
MethodSequencing
Analysis
Platform
Comments
ReferenceQuan_et_al_2021
Pubmed ID34034800
Accession Number(s)nsv4749746
Frequency
Sample Size25
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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