A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5413989



Internal ID193277
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr1:155020589..155021910hg38UCSC Ensembl
chr1:154993065..154994386hg19UCSC Ensembl
Cytoband1q21.3
Allele length
AssemblyAllele length
hg381322
hg191322
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv16890424
Samples
Known GenesDCST2
MethodSequencing
Analysis
Platform
Comments
ReferenceByrska_Bishop_et_al_2022
Pubmed ID36055201
Accession Number(s)nsv5413989
Frequency
Sample Size3202
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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