A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5557398



Internal ID330497
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr10:119401020..119409668hg38UCSC Ensembl
chr10:121160532..121169180hg19UCSC Ensembl
Cytoband10q26.11
Allele length
AssemblyAllele length
hg388649
hg198649
Variant TypeOTHER sequence alteration
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17039317
Samples
Known GenesGRK5
MethodSequencing
Analysis
Platform
Commentscomplex variant
ReferenceByrska_Bishop_et_al_2022
Pubmed ID36055201
Accession Number(s)nsv5557398
Frequency
Sample Size3202
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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