A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6379649



Internal ID21037202
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr4:69956801..69957800hg38UCSC Ensembl
chr4:70822519..70823518hg19UCSC Ensembl
Cytoband4q13.3
Allele length
AssemblyAllele length
hg381000
hg191000
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18211704
Samples
Known GenesCSN2
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6379649
Frequency
Sample Size19652
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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