A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17523676



Internal ID21848035
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr2:75154434..75154488hg38UCSC Ensembl
chr2:75381560..75381614hg19UCSC Ensembl
Cytoband2p12
Allele length
AssemblyAllele length
hg3855
hg1955
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv5989905
Supporting Variants
Samples
Known GenesTACR1
MethodSequencing
Analysis
Platform
Comments
ReferenceWu_et_al_2021
Pubmed ID34764282
Accession Number(s)nssv17523676
Frequency
Sample Size405
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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