A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17576824



Internal ID21768867
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr6:39284874..39284943hg38UCSC Ensembl
chr6:39252650..39252719hg19UCSC Ensembl
Cytoband6p21.2
Allele length
AssemblyAllele length
hg3870
hg1970
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6009870
Supporting Variants
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceWu_et_al_2021
Pubmed ID34764282
Accession Number(s)nssv17576824
Frequency
Sample Size405
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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