A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6368303



Internal ID21025856
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr3:185167326..185173030hg38UCSC Ensembl
chr3:184885114..184890818hg19UCSC Ensembl
Cytoband3q27.2
Allele length
AssemblyAllele length
hg385705
hg195705
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18097662
Samples
Known GenesEHHADH-AS1
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6368303
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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