A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5843906



Internal ID22618841
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr5:95607719..95608949hg38UCSC Ensembl
chr5:94943423..94944653hg19UCSC Ensembl
Cytoband5q15
Allele length
AssemblyAllele length
hg381231
hg191231
Variant TypeOTHER complex
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17500118
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceAlmarri_et_al_2020
Pubmed ID32531199
Accession Number(s)nsv5843906
Frequency
Sample Size914
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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