A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5858136



Internal ID22633071
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr14:39536675..39542074hg38UCSC Ensembl
chr14:40005879..40011278hg19UCSC Ensembl
Cytoband14q21.1
Allele length
AssemblyAllele length
hg385400
hg195400
Variant TypeOTHER complex
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17468422, nssv17450870
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceAlmarri_et_al_2020
Pubmed ID32531199
Accession Number(s)nsv5858136
Frequency
Sample Size914
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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