A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6364492



Internal ID21022045
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr3:18431143..18434570hg38UCSC Ensembl
chr3:18472635..18476062hg19UCSC Ensembl
Cytoband3p24.3
Allele length
AssemblyAllele length
hg383428
hg193428
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18097594
Samples
Known GenesSATB1
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6364492
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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