A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17558652



Internal ID21883007
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr6:127651219..127770775hg38UCSC Ensembl
chr6:127972364..128091920hg19UCSC Ensembl
Cytoband6q22.33
Allele length
AssemblyAllele length
hg38119557
hg19119557
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6016459
Supporting Variants
Samples
Known GenesTHEMIS
MethodSequencing
Analysis
Platform
Comments
ReferenceWu_et_al_2021
Pubmed ID34764282
Accession Number(s)nssv17558652
Frequency
Sample Size405
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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