A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5848681



Internal ID22623616
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr10:20855755..20857154hg38UCSC Ensembl
chr10:21144684..21146083hg19UCSC Ensembl
Cytoband10p12.31
Allele length
AssemblyAllele length
hg381400
hg191400
Variant TypeOTHER complex
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17459497
Samples
Known GenesNEBL
MethodSequencing
Analysis
Platform
Comments
ReferenceAlmarri_et_al_2020
Pubmed ID32531199
Accession Number(s)nsv5848681
Frequency
Sample Size914
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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