A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17573741



Internal ID21765784
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr6:8281024..8281169hg38UCSC Ensembl
chr6:8281257..8281402hg19UCSC Ensembl
Cytoband6p24.3
Allele length
AssemblyAllele length
hg38146
hg19146
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6017774
Supporting Variants
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceWu_et_al_2021
Pubmed ID34764282
Accession Number(s)nssv17573741
Frequency
Sample Size405
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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