A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6415058



Internal ID21072611
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr6:36327400..36339808hg38UCSC Ensembl
chr6:36295177..36307585hg19UCSC Ensembl
Cytoband6p21.31
Allele length
AssemblyAllele length
hg3812409
hg1912409
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18141745
Samples
Known GenesC6orf222
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6415058
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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