A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6393400



Internal ID21050953
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr4:146220219..146289001hg38UCSC Ensembl
chr4:147141371..147210153hg19UCSC Ensembl
Cytoband4q31.22
Allele length
AssemblyAllele length
hg3868783
hg1968783
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18212029
Samples
Known GenesSLC10A7
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6393400
Frequency
Sample Size19652
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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