A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6377585



Internal ID21035138
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr4:89045025..89135859hg38UCSC Ensembl
chr4:89966176..90057010hg19UCSC Ensembl
Cytoband4q22.1
Allele length
AssemblyAllele length
hg3890835
hg1990835
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18214778
Samples
Known GenesFAM13A, TIGD2
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6377585
Frequency
Sample Size19652
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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