A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5835054



Internal ID22609989
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr3:159735128..159736127hg38UCSC Ensembl
chr3:159452917..159453916hg19UCSC Ensembl
Cytoband3q25.33
Allele length
AssemblyAllele length
hg381000
hg191000
Variant TypeOTHER complex
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17486507
Samples
Known GenesIQCJ-SCHIP1, SCHIP1
MethodSequencing
Analysis
Platform
Comments
ReferenceAlmarri_et_al_2020
Pubmed ID32531199
Accession Number(s)nsv5835054
Frequency
Sample Size914
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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