A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv16900650



Internal ID1224
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr1:39068317..39074240hg38UCSC Ensembl
chr1:39533989..39539912hg19UCSC Ensembl
Cytoband1p34.3
Allele length
AssemblyAllele length
hg385924
hg195924
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6138973
Supporting Variants
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceByrska_Bishop_et_al_2022
Pubmed ID36055201
Accession Number(s)nssv16900650
Frequency
Sample Size3202
Observed Gain1
Observed Loss0
Observed Complex0
Frequency0.00203


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