A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6610118



Internal ID20983189
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr6:116910218..116910665hg38UCSC Ensembl
chr6:117231381..117231828hg19UCSC Ensembl
Cytoband6q22.1
Allele length
AssemblyAllele length
hg38448
hg19448
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18137194
Samples
Known GenesRFX6
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6610118
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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