A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv4734744



Internal ID20510682
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr2:19006854..19022984hg38UCSC Ensembl
chr2:19188127..19206631hg19UCSC Ensembl
Cytoband2p24.1
Allele length
AssemblyAllele length
hg3816131
hg1918505
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv16270076
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceQuan_et_al_2021
Pubmed ID34034800
Accession Number(s)nsv4734744
Frequency
Sample Size25
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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