A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv16903386



Internal ID3069
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr1:56059400..56059451hg38UCSC Ensembl
chr1:56525073..56525124hg19UCSC Ensembl
Cytoband1p32.2
Allele length
AssemblyAllele length
hg382937
hg192937
Variant TypeCNV line1 insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv5556439
Supporting Variants
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceByrska_Bishop_et_al_2022
Pubmed ID36055201
Accession Number(s)nssv16903386
Frequency
Sample Size3202
Observed Gain1
Observed Loss0
Observed Complex0
Frequency0.002187


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