A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5427363



Internal ID206268
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr1:150623884..150625144hg38UCSC Ensembl
chr1:150596360..150597620hg19UCSC Ensembl
Cytoband1q21.3
Allele length
AssemblyAllele length
hg381261
hg191261
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv16890589
Samples
Known GenesENSA
MethodSequencing
Analysis
Platform
Comments
ReferenceByrska_Bishop_et_al_2022
Pubmed ID36055201
Accession Number(s)nsv5427363
Frequency
Sample Size3202
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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