A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17518069



Internal ID21842428
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr2:965248..965365hg38UCSC Ensembl
chr2:960934..961051hg19UCSC Ensembl
Cytoband2p25.3
Allele length
AssemblyAllele length
hg38118
hg19118
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv5990693
Supporting Variants
Samples
Known GenesSNTG2
MethodSequencing
Analysis
Platform
Comments
ReferenceWu_et_al_2021
Pubmed ID34764282
Accession Number(s)nssv17518069
Frequency
Sample Size405
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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