A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6379585



Internal ID21037138
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr4:150255578..150258371hg38UCSC Ensembl
chr4:151176730..151179523hg19UCSC Ensembl
Cytoband4q31.3
Allele length
AssemblyAllele length
hg382794
hg192794
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18212070
Samples
Known GenesDCLK2
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6379585
Frequency
Sample Size19652
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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