A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5827638



Internal ID22602568
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr1:125137724..125141699hg38UCSC Ensembl
Cytoband
Allele length
AssemblyAllele length
hg383976
Variant TypeOTHER complex
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17455262, nssv17467420
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceAlmarri_et_al_2020
Pubmed ID32531199
Accession Number(s)nsv5827638
Frequency
Sample Size914
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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