A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6385461



Internal ID21043014
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr4:153325750..153352114hg38UCSC Ensembl
chr4:154246902..154273266hg19UCSC Ensembl
Cytoband4q31.3
Allele length
AssemblyAllele length
hg3826365
hg1926365
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18212109
Samples
Known GenesMND1, TRIM2
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6385461
Frequency
Sample Size19652
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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