A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5843951



Internal ID22618886
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr6:103491422..103495327hg38UCSC Ensembl
chr6:103939297..103943202hg19UCSC Ensembl
Cytoband6q16.3
Allele length
AssemblyAllele length
hg383906
hg193906
Variant TypeOTHER complex
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv1798n209
Supporting Variantsnssv17500277
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceAlmarri_et_al_2020
Pubmed ID32531199
Accession Number(s)nsv5843951
Frequency
Sample Size914
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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