A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5554188



Internal ID327384
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr11:101251729..101252554hg38UCSC Ensembl
chr11:101122460..101123285hg19UCSC Ensembl
Cytoband11q22.1
Allele length
AssemblyAllele length
hg38826
hg19826
Variant TypeOTHER sequence alteration
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17051309
Samples
Known Genes
MethodSequencing
Analysis
Platform
Commentscomplex variant
ReferenceByrska_Bishop_et_al_2022
Pubmed ID36055201
Accession Number(s)nsv5554188
Frequency
Sample Size3202
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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