A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6600511



Internal ID20973582
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr6:110672401..110673600hg38UCSC Ensembl
chr6:110993604..110994803hg19UCSC Ensembl
Cytoband6q21
Allele length
AssemblyAllele length
hg381200
hg191200
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18136685
Samples
Known GenesCDK19
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6600511
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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