A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5912184



Internal ID22687400
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr10:62064578..62065761hg38UCSC Ensembl
chr10:63824337..63825520hg19UCSC Ensembl
Cytoband10q21.2
Allele length
AssemblyAllele length
hg381184
hg191184
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17364705
Samples
Known GenesARID5B
MethodSequencing
Analysis
Platform
Comments
ReferenceAlmarri_et_al_2020
Pubmed ID32531199
Accession Number(s)nsv5912184
Frequency
Sample Size914
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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