A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17598201



Internal ID21790245
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr12:25928116..25928214hg38UCSC Ensembl
chr12:26081049..26081147hg19UCSC Ensembl
Cytoband12p12.1
Allele length
AssemblyAllele length
hg3899
hg1999
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6027625
Supporting Variants
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceWu_et_al_2021
Pubmed ID34764282
Accession Number(s)nssv17598201
Frequency
Sample Size405
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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