A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5828544



Internal ID22603479
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr1:172314362..172316220hg38UCSC Ensembl
chr1:172283502..172285360hg19UCSC Ensembl
Cytoband1q24.3
Allele length
AssemblyAllele length
hg381859
hg191859
Variant TypeOTHER complex
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17454743, nssv17451594
Samples
Known GenesDNM3
MethodSequencing
Analysis
Platform
Comments
ReferenceAlmarri_et_al_2020
Pubmed ID32531199
Accession Number(s)nsv5828544
Frequency
Sample Size914
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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