A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6393382



Internal ID21050935
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr4:82898101..82900100hg38UCSC Ensembl
chr4:83819254..83821253hg19UCSC Ensembl
Cytoband4q21.22
Allele length
AssemblyAllele length
hg382000
hg192000
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18214717
Samples
Known GenesTHAP9-AS1
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6393382
Frequency
Sample Size19652
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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