A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17526348



Internal ID21850706
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr2:237868057..237882997hg38UCSC Ensembl
chr2:238776700..238791639hg19UCSC Ensembl
Cytoband2q37.3
Allele length
AssemblyAllele length
hg3814941
hg1914940
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv5988050
Supporting Variants
Samples
Known GenesRAMP1
MethodSequencing
Analysis
Platform
Comments
ReferenceWu_et_al_2021
Pubmed ID34764282
Accession Number(s)nssv17526348
Frequency
Sample Size405
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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