A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5558125



Internal ID331198
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr2:7326172..7327374hg38UCSC Ensembl
chr2:7466303..7467505hg19UCSC Ensembl
Cytoband2p25.1
Allele length
AssemblyAllele length
hg381203
hg191203
Variant TypeOTHER sequence alteration
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv16909364
Samples
Known Genes
MethodSequencing
Analysis
Platform
Commentscomplex variant
ReferenceByrska_Bishop_et_al_2022
Pubmed ID36055201
Accession Number(s)nsv5558125
Frequency
Sample Size3202
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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