A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5829934



Internal ID22604869
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr1:26847071..26860492hg38UCSC Ensembl
chr1:27173562..27186983hg19UCSC Ensembl
Cytoband1p36.11
Allele length
AssemblyAllele length
hg3813422
hg1913422
Variant TypeOTHER complex
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17454912
Samples
Known GenesZDHHC18
MethodSequencing
Analysis
Platform
Comments
ReferenceAlmarri_et_al_2020
Pubmed ID32531199
Accession Number(s)nsv5829934
Frequency
Sample Size914
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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