A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17557627



Internal ID21881982
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr6:142862434..142862507hg38UCSC Ensembl
chr6:143183571..143183644hg19UCSC Ensembl
Cytoband6q24.2
Allele length
AssemblyAllele length
hg3874
hg1974
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6009024
Supporting Variants
Samples
Known GenesHIVEP2
MethodSequencing
Analysis
Platform
Comments
ReferenceWu_et_al_2021
Pubmed ID34764282
Accession Number(s)nssv17557627
Frequency
Sample Size405
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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