A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5828705



Internal ID22603640
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr1:161916691..161984740hg38UCSC Ensembl
chr1:161886481..161954530hg19UCSC Ensembl
Cytoband1q23.3
Allele length
AssemblyAllele length
hg3868050
hg1968050
Variant TypeOTHER complex
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17458640
Samples
Known GenesATF6, OLFML2B
MethodSequencing
Analysis
Platform
Comments
ReferenceAlmarri_et_al_2020
Pubmed ID32531199
Accession Number(s)nsv5828705
Frequency
Sample Size914
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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