A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6405809



Internal ID21063362
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr6:42098327..42103111hg38UCSC Ensembl
chr6:42066065..42070849hg19UCSC Ensembl
Cytoband6p21.1
Allele length
AssemblyAllele length
hg384785
hg194785
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18143360
Samples
Known GenesC6orf132
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6405809
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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