A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv4736891



Internal ID20512845
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr2:70325430..70325618hg38UCSC Ensembl
chr2:70552562..70552750hg19UCSC Ensembl
Cytoband2p13.3
Allele length
AssemblyAllele length
hg38189
hg19189
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv16267158
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceQuan_et_al_2021
Pubmed ID34034800
Accession Number(s)nsv4736891
Frequency
Sample Size25
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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