A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17617296



Internal ID21809343
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr12:56287488..56293445hg38UCSC Ensembl
chr12:56681272..56687229hg19UCSC Ensembl
Cytoband12q13.3
Allele length
AssemblyAllele length
hg385958
hg195958
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6027906
Supporting Variants
Samples
Known GenesCS
MethodSequencing
Analysis
Platform
Comments
ReferenceWu_et_al_2021
Pubmed ID34764282
Accession Number(s)nssv17617296
Frequency
Sample Size405
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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