A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5562131



Internal ID335090
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr1:212658794..212663951hg38UCSC Ensembl
chr1:212832136..212837293hg19UCSC Ensembl
Cytoband1q32.3
Allele length
AssemblyAllele length
hg385158
hg195158
Variant TypeOTHER sequence alteration
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv16895735
Samples
Known Genes
MethodSequencing
Analysis
Platform
Commentscomplex variant
ReferenceByrska_Bishop_et_al_2022
Pubmed ID36055201
Accession Number(s)nsv5562131
Frequency
Sample Size3202
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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