A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17570644



Internal ID21762687
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr6:88353708..88357171hg38UCSC Ensembl
chr6:89063427..89066890hg19UCSC Ensembl
Cytoband6q15
Allele length
AssemblyAllele length
hg383464
hg193464
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6012987
Supporting Variants
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceWu_et_al_2021
Pubmed ID34764282
Accession Number(s)nssv17570644
Frequency
Sample Size405
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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