A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv4734506



Internal ID20510443
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr2:57482451..57482531hg38UCSC Ensembl
chr2:57709586..57709666hg19UCSC Ensembl
Cytoband2p16.1
Allele length
AssemblyAllele length
hg3881
hg1981
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv16290806
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceQuan_et_al_2021
Pubmed ID34034800
Accession Number(s)nsv4734506
Frequency
Sample Size25
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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