A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6371619



Internal ID21029172
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr3:24399601..24428400hg38UCSC Ensembl
chr3:24441092..24469891hg19UCSC Ensembl
Cytoband3p24.2
Allele length
AssemblyAllele length
hg3828800
hg1928800
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv4823n223
Supporting Variantsnssv18101034
Samples
Known GenesTHRB
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6371619
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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