A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6375062



Internal ID21032615
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr3:23980601..23982600hg38UCSC Ensembl
chr3:24022092..24024091hg19UCSC Ensembl
Cytoband3p24.2
Allele length
AssemblyAllele length
hg382000
hg192000
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18100400
Samples
Known GenesNR1D2
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6375062
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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