A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6393457



Internal ID21051010
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr4:96183107..96264141hg38UCSC Ensembl
chr4:97104258..97185292hg19UCSC Ensembl
Cytoband4q22.3
Allele length
AssemblyAllele length
hg3881035
hg1981035
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18214352
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6393457
Frequency
Sample Size19652
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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