A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6398901



Internal ID21056454
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr6:24372265..24384132hg38UCSC Ensembl
chr6:24372493..24384360hg19UCSC Ensembl
Cytoband6p22.3
Allele length
AssemblyAllele length
hg3811868
hg1911868
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18221117
Samples
Known GenesDCDC2
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6398901
Frequency
Sample Size19652
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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