A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5432662



Internal ID211400
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr1:102190302..102393130hg38UCSC Ensembl
chr1:102655858..102858686hg19UCSC Ensembl
Cytoband1p21.1
Allele length
AssemblyAllele length
hg38202829
hg19202829
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv16908661
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceByrska_Bishop_et_al_2022
Pubmed ID36055201
Accession Number(s)nsv5432662
Frequency
Sample Size3202
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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