A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17528235



Internal ID21852592
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr2:84934262..84935502hg38UCSC Ensembl
chr2:85161386..85162626hg19UCSC Ensembl
Cytoband2p11.2
Allele length
AssemblyAllele length
hg381241
hg191241
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv5990075
Supporting Variants
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceWu_et_al_2021
Pubmed ID34764282
Accession Number(s)nssv17528235
Frequency
Sample Size405
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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