A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5862538



Internal ID22637473
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr10:62064460..62065796hg38UCSC Ensembl
chr10:63824219..63825555hg19UCSC Ensembl
Cytoband10q21.2
Allele length
AssemblyAllele length
hg381337
hg191337
Variant TypeOTHER complex
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17459910
Samples
Known GenesARID5B
MethodSequencing
Analysis
Platform
Comments
ReferenceAlmarri_et_al_2020
Pubmed ID32531199
Accession Number(s)nsv5862538
Frequency
Sample Size914
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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