A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5426717



Internal ID205641
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr1:151022309..151022568hg38UCSC Ensembl
chr1:150994785..150995044hg19UCSC Ensembl
Cytoband1q21.3
Allele length
AssemblyAllele length
hg38260
hg19260
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv16889211
Samples
Known GenesPRUNE
MethodSequencing
Analysis
Platform
Comments
ReferenceByrska_Bishop_et_al_2022
Pubmed ID36055201
Accession Number(s)nsv5426717
Frequency
Sample Size3202
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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