A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17565612



Internal ID21757577
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr6:104774080..104774393hg38UCSC Ensembl
chr6:105221955..105222268hg19UCSC Ensembl
Cytoband6q16.3
Allele length
AssemblyAllele length
hg38314
hg19314
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6007576
Supporting Variants
Samples
Known GenesHACE1
MethodSequencing
Analysis
Platform
Comments
ReferenceWu_et_al_2021
Pubmed ID34764282
Accession Number(s)nssv17565612
Frequency
Sample Size405
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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