A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6405838



Internal ID21063391
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr6:1884170..1910211hg38UCSC Ensembl
chr6:1884404..1910445hg19UCSC Ensembl
Cytoband6p25.3
Allele length
AssemblyAllele length
hg3826042
hg1926042
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18143091
Samples
Known GenesGMDS
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6405838
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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