A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6365907



Internal ID21023460
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr3:97787436..97787960hg38UCSC Ensembl
chr3:97506280..97506804hg19UCSC Ensembl
Cytoband3q11.2
Allele length
AssemblyAllele length
hg38525
hg19525
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18105540
Samples
Known GenesARL6
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6365907
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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