A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5417696



Internal ID196887
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr1:119657533..119670989hg38UCSC Ensembl
chr1:120200156..120213612hg19UCSC Ensembl
Cytoband1p12
Allele length
AssemblyAllele length
hg3813457
hg1913457
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv16889005
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceByrska_Bishop_et_al_2022
Pubmed ID36055201
Accession Number(s)nsv5417696
Frequency
Sample Size3202
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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