A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6400726



Internal ID21058279
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr6:93725889..93821568hg38UCSC Ensembl
chr6:94435607..94531286hg19UCSC Ensembl
Cytoband6q16.1
Allele length
AssemblyAllele length
hg3895680
hg1995680
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18146870
Samples
Known GenesTSG1
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6400726
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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