A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6404429



Internal ID21061982
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr6:10354649..10380353hg38UCSC Ensembl
chr6:10354882..10380586hg19UCSC Ensembl
Cytoband6p24.3
Allele length
AssemblyAllele length
hg3825705
hg1925705
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18135978
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6404429
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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