A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5555306



Internal ID328466
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr2:62384663..62390334hg38UCSC Ensembl
chr2:62611798..62617469hg19UCSC Ensembl
Cytoband2p15
Allele length
AssemblyAllele length
hg385672
hg195672
Variant TypeOTHER sequence alteration
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv16913880
Samples
Known Genes
MethodSequencing
Analysis
Platform
Commentscomplex variant
ReferenceByrska_Bishop_et_al_2022
Pubmed ID36055201
Accession Number(s)nsv5555306
Frequency
Sample Size3202
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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