A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6387456



Internal ID21045009
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr4:150141293..150141675hg38UCSC Ensembl
chr4:151062445..151062827hg19UCSC Ensembl
Cytoband4q31.23
Allele length
AssemblyAllele length
hg38383
hg19383
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18112255
Samples
Known GenesDCLK2
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6387456
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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