A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6402406



Internal ID21059959
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr6:13358367..13362533hg38UCSC Ensembl
chr6:13358599..13362765hg19UCSC Ensembl
Cytoband6p24.1
Allele length
AssemblyAllele length
hg384167
hg194167
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18139381
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6402406
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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