A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17573969



Internal ID21766012
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr6:108077999..108082646hg38UCSC Ensembl
chr6:108399203..108403850hg19UCSC Ensembl
Cytoband6q21
Allele length
AssemblyAllele length
hg384648
hg194648
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6010283
Supporting Variants
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceWu_et_al_2021
Pubmed ID34764282
Accession Number(s)nssv17573969
Frequency
Sample Size405
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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