A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6404691



Internal ID21062244
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr6:26587795..26601188hg38UCSC Ensembl
chr6:26588023..26601416hg19UCSC Ensembl
Cytoband6p22.2
Allele length
AssemblyAllele length
hg3813394
hg1913394
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18140760
Samples
Known GenesABT1
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6404691
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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