A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5562781



Internal ID335725
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr10:88183870..88689203hg38UCSC Ensembl
chr10:89943627..90448960hg19UCSC Ensembl
Cytoband10q23.31
Allele length
AssemblyAllele length
hg38505334
hg19505334
Variant TypeOTHER sequence alteration
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17038419
Samples
Known GenesLIPF, LIPJ, RNLS
MethodSequencing
Analysis
Platform
Commentscomplex variant
ReferenceByrska_Bishop_et_al_2022
Pubmed ID36055201
Accession Number(s)nsv5562781
Frequency
Sample Size3202
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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