A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6611341



Internal ID20984412
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr6:108885027..108886328hg38UCSC Ensembl
chr6:109206230..109207531hg19UCSC Ensembl
Cytoband6q21
Allele length
AssemblyAllele length
hg381302
hg191302
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18137010
Samples
Known GenesARMC2
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6611341
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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