A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6364831



Internal ID21022384
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr3:40669485..40673386hg38UCSC Ensembl
chr3:40710976..40714877hg19UCSC Ensembl
Cytoband3p22.1
Allele length
AssemblyAllele length
hg383902
hg193902
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18099157
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6364831
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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