A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5435877



Internal ID214507
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr2:73275859..73276887hg38UCSC Ensembl
chr2:73502987..73504015hg19UCSC Ensembl
Cytoband2p13.1
Allele length
AssemblyAllele length
hg381029
hg191029
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv16915438
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceByrska_Bishop_et_al_2022
Pubmed ID36055201
Accession Number(s)nsv5435877
Frequency
Sample Size3202
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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