A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6368038



Internal ID21025591
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr3:144148879..144308271hg38UCSC Ensembl
chr3:143867721..144027113hg19UCSC Ensembl
Cytoband3q24
Allele length
AssemblyAllele length
hg38159393
hg19159393
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18095006
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6368038
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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