A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5416655



Internal ID195876
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 StatusM
Merged Variants
Supporting Variantsnssv16902064
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceByrska_Bishop_et_al_2022
Pubmed ID36055201
Accession Number(s)nsv5416655
Frequency
Sample Size3202
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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