A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17537084



Internal ID21861439
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr2:53671695..53671877hg38UCSC Ensembl
chr2:53898832..53899014hg19UCSC Ensembl
Cytoband2p16.2
Allele length
AssemblyAllele length
hg38183
hg19183
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv5989502
Supporting Variants
Samples
Known GenesASB3, GPR75-ASB3
MethodSequencing
Analysis
Platform
Comments
ReferenceWu_et_al_2021
Pubmed ID34764282
Accession Number(s)nssv17537084
Frequency
Sample Size405
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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