A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17569549



Internal ID21761592
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr8:38100982..38101081hg38UCSC Ensembl
chr8:37958500..37958599hg19UCSC Ensembl
Cytoband8p11.23
Allele length
AssemblyAllele length
hg38100
hg19100
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6005421
Supporting Variants
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceWu_et_al_2021
Pubmed ID34764282
Accession Number(s)nssv17569549
Frequency
Sample Size405
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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