A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv16981940



Internal ID55318
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr6:32017950..32023500hg38UCSC Ensembl
chr6:31985727..31991277hg19UCSC Ensembl
Cytoband6p21.33
Allele length
AssemblyAllele length
hg385551
hg195551
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6141332
Supporting Variants
Samples
Known GenesC4A, C4B, C4B_2
MethodSequencing
Analysis
Platform
Comments
ReferenceByrska_Bishop_et_al_2022
Pubmed ID36055201
Accession Number(s)nssv16981940
Frequency
Sample Size3202
Observed Gain1
Observed Loss0
Observed Complex0
Frequency0.019053


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