A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5835018



Internal ID22609953
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr3:160177630..160182097hg38UCSC Ensembl
chr3:159895417..159899884hg19UCSC Ensembl
Cytoband3q25.33
Allele length
AssemblyAllele length
hg384468
hg194468
Variant TypeOTHER complex
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17486513
Samples
Known GenesIL12A-AS1
MethodSequencing
Analysis
Platform
Comments
ReferenceAlmarri_et_al_2020
Pubmed ID32531199
Accession Number(s)nsv5835018
Frequency
Sample Size914
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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