A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6607681



Internal ID20980752
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr6:123268635..123269140hg38UCSC Ensembl
chr6:123589780..123590285hg19UCSC Ensembl
Cytoband6q22.31
Allele length
AssemblyAllele length
hg38506
hg19506
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18137455
Samples
Known GenesTRDN
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6607681
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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