A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6601878



Internal ID20974949
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr6:116536113..116536805hg38UCSC Ensembl
chr6:116857276..116857968hg19UCSC Ensembl
Cytoband6q22.1
Allele length
AssemblyAllele length
hg38693
hg19693
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18137154
Samples
Known GenesFAM26D, TRAPPC3L
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6601878
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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