A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6372550



Internal ID21030103
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr3:158707701..158711300hg38UCSC Ensembl
chr3:158425490..158429089hg19UCSC Ensembl
Cytoband3q25.32
Allele length
AssemblyAllele length
hg383600
hg193600
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18094638
Samples
Known GenesRARRES1
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6372550
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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