A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv16901299



Internal ID1678
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr1:30871056..30871913hg38UCSC Ensembl
chr1:31343903..31344760hg19UCSC Ensembl
Cytoband1p35.2
Allele length
AssemblyAllele length
hg38858
hg19858
Variant TypeOTHER sequence alteration
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv5557604
Supporting Variants
Samples
Known GenesSDC3
MethodSequencing
Analysis
Platform
Commentscomplex variant
ReferenceByrska_Bishop_et_al_2022
Pubmed ID36055201
Accession Number(s)nssv16901299
Frequency
Sample Size3202
Observed Gain0
Observed Loss0
Observed Complex0
Frequency0.000156


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