A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5836578



Internal ID22611513
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr3:47327789..47328788hg38UCSC Ensembl
chr3:47369279..47370278hg19UCSC Ensembl
Cytoband3p21.31
Allele length
AssemblyAllele length
hg381000
hg191000
Variant TypeOTHER complex
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17491573, nssv17491574
Samples
Known GenesKLHL18
MethodSequencing
Analysis
Platform
Comments
ReferenceAlmarri_et_al_2020
Pubmed ID32531199
Accession Number(s)nsv5836578
Frequency
Sample Size914
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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