A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv16903738



Internal ID3309
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr1:37076827..37094499hg38UCSC Ensembl
chr1:37542428..37560100hg19UCSC Ensembl
Cytoband1p34.3
Allele length
AssemblyAllele length
hg3817673
hg1917673
Variant TypeOTHER sequence alteration
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv5562171
Supporting Variants
Samples
Known Genes
MethodSequencing
Analysis
Platform
Commentscomplex variant
ReferenceByrska_Bishop_et_al_2022
Pubmed ID36055201
Accession Number(s)nssv16903738
Frequency
Sample Size3202
Observed Gain0
Observed Loss0
Observed Complex0
Frequency0.000312


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