A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6364871



Internal ID21022424
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr3:94015401..94016500hg38UCSC Ensembl
chr3:93734245..93735344hg19UCSC Ensembl
Cytoband3q11.1
Allele length
AssemblyAllele length
hg381100
hg191100
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18106676
Samples
Known GenesARL13B, STX19
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6364871
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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