A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5425755



Internal ID204711
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr1:39055457..39055899hg38UCSC Ensembl
chr1:39521129..39521571hg19UCSC Ensembl
Cytoband1p34.3
Allele length
AssemblyAllele length
hg38443
hg19443
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv16900649
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceByrska_Bishop_et_al_2022
Pubmed ID36055201
Accession Number(s)nsv5425755
Frequency
Sample Size3202
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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