A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv18229885



Internal ID20796926
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr8:103234434..103238723hg38UCSC Ensembl
chr8:104246662..104250951hg19UCSC Ensembl
Cytoband8q22.3
Allele length
AssemblyAllele length
hg384290
hg194290
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6418546
Supporting Variants
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nssv18229885
Frequency
Sample Size19652
Observed Gain1
Observed Loss0
Observed Complex0
Frequency0.00071


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