A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17602560



Internal ID21794607
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr12:89943046..89948912hg38UCSC Ensembl
chr12:90336823..90342689hg19UCSC Ensembl
Cytoband12q21.33
Allele length
AssemblyAllele length
hg385867
hg195867
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6023089
Supporting Variants
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceWu_et_al_2021
Pubmed ID34764282
Accession Number(s)nssv17602560
Frequency
Sample Size405
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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