A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17583357



Internal ID21775400
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr8:138206329..138206384hg38UCSC Ensembl
chr8:139218572..139218627hg19UCSC Ensembl
Cytoband8q24.23
Allele length
AssemblyAllele length
hg3856
hg1956
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6008648
Supporting Variants
Samples
Known GenesFAM135B
MethodSequencing
Analysis
Platform
Comments
ReferenceWu_et_al_2021
Pubmed ID34764282
Accession Number(s)nssv17583357
Frequency
Sample Size405
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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