A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5828363



Internal ID22603298
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr1:155546981..155548985hg38UCSC Ensembl
chr1:155516772..155518776hg19UCSC Ensembl
Cytoband1q22
Allele length
AssemblyAllele length
hg382005
hg192005
Variant TypeOTHER complex
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17455728
Samples
Known GenesASH1L
MethodSequencing
Analysis
Platform
Comments
ReferenceAlmarri_et_al_2020
Pubmed ID32531199
Accession Number(s)nsv5828363
Frequency
Sample Size914
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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