A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv16902064



Internal ID2173
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr1:37802178..37802398hg38UCSC Ensembl
chr1:38267850..38268070hg19UCSC Ensembl
Cytoband1p34.3
Allele length
AssemblyAllele length
hg38221
hg19221
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv5416655
Supporting Variants
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceByrska_Bishop_et_al_2022
Pubmed ID36055201
Accession Number(s)nssv16902064
Frequency
Sample Size3202
Observed Gain0
Observed Loss1
Observed Complex0
Frequency0.000781


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