A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17577228



Internal ID21769271
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr6:135255637..135261025hg38UCSC Ensembl
chr6:135576775..135582163hg19UCSC Ensembl
Cytoband6q23.3
Allele length
AssemblyAllele length
hg385389
hg195389
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6005246
Supporting Variants
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceWu_et_al_2021
Pubmed ID34764282
Accession Number(s)nssv17577228
Frequency
Sample Size405
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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