A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6605692



Internal ID20978763
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr6:123533073..123542795hg38UCSC Ensembl
chr6:123854218..123863940hg19UCSC Ensembl
Cytoband6q22.31
Allele length
AssemblyAllele length
hg389723
hg199723
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18137494
Samples
Known GenesTRDN
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6605692
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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