A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5985931



Internal ID21895274
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr2:127788892..127788974hg38UCSC Ensembl
chr2:128546466..128546548hg19UCSC Ensembl
Cytoband2q14.3
Allele length
AssemblyAllele length
hg3883
hg1983
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17522308
Samples
Known GenesWDR33
MethodSequencing
Analysis
Platform
Comments
ReferenceWu_et_al_2021
Pubmed ID34764282
Accession Number(s)nsv5985931
Frequency
Sample Size405
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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