A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17559059



Internal ID21883414
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr6:88283186..88283246hg38UCSC Ensembl
chr6:88992905..88992965hg19UCSC Ensembl
Cytoband6q15
Allele length
AssemblyAllele length
hg3861
hg1961
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6013469
Supporting Variants
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceWu_et_al_2021
Pubmed ID34764282
Accession Number(s)nssv17559059
Frequency
Sample Size405
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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