A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5434728



Internal ID213397
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr2:31687231..31691164hg38UCSC Ensembl
chr2:31912300..31916233hg19UCSC Ensembl
Cytoband2p23.1
Allele length
AssemblyAllele length
hg383934
hg193934
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv16910734
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceByrska_Bishop_et_al_2022
Pubmed ID36055201
Accession Number(s)nsv5434728
Frequency
Sample Size3202
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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