A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17563232



Internal ID21887587
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr6:107953755..107953856hg38UCSC Ensembl
chr6:108274959..108275060hg19UCSC Ensembl
Cytoband6q21
Allele length
AssemblyAllele length
hg38102
hg19102
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6001498
Supporting Variants
Samples
Known GenesSEC63
MethodSequencing
Analysis
Platform
Comments
ReferenceWu_et_al_2021
Pubmed ID34764282
Accession Number(s)nssv17563232
Frequency
Sample Size405
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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