A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv4738914



Internal ID20514885
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr2:212939398..212939608hg38UCSC Ensembl
chr2:213804122..213804332hg19UCSC Ensembl
Cytoband2q34
Allele length
AssemblyAllele length
hg38211
hg19211
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv16272386
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceQuan_et_al_2021
Pubmed ID34034800
Accession Number(s)nsv4738914
Frequency
Sample Size25
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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