A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5558999



Internal ID332047
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr2:187946302..188035547hg38UCSC Ensembl
chr2:188811029..188900274hg19UCSC Ensembl
Cytoband2q32.1
Allele length
AssemblyAllele length
hg3889246
hg1989246
Variant TypeOTHER sequence alteration
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv16921972
Samples
Known Genes
MethodSequencing
Analysis
Platform
Commentscomplex variant
ReferenceByrska_Bishop_et_al_2022
Pubmed ID36055201
Accession Number(s)nsv5558999
Frequency
Sample Size3202
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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