A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5556977



Internal ID330095
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr3:183639349..183716202hg38UCSC Ensembl
chr3:183357137..183433990hg19UCSC Ensembl
Cytoband3q27.1
Allele length
AssemblyAllele length
hg3876854
hg1976854
Variant TypeOTHER sequence alteration
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv16944758
Samples
Known GenesKLHL24, YEATS2
MethodSequencing
Analysis
Platform
Commentscomplex variant
ReferenceByrska_Bishop_et_al_2022
Pubmed ID36055201
Accession Number(s)nsv5556977
Frequency
Sample Size3202
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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