A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6381405



Internal ID21038958
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr4:48112741..48121315hg38UCSC Ensembl
chr4:48114758..48123332hg19UCSC Ensembl
Cytoband4p12
Allele length
AssemblyAllele length
hg388575
hg198575
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18117268
Samples
Known GenesTXK
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6381405
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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