A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6396333



Internal ID21053886
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr6:24553407..24555903hg38UCSC Ensembl
chr6:24553635..24556131hg19UCSC Ensembl
Cytoband6p22.3
Allele length
AssemblyAllele length
hg382497
hg192497
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18140662
Samples
Known GenesKIAA0319
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6396333
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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