A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6602316



Internal ID20975387
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr6:134730267..134731495hg38UCSC Ensembl
chr6:135051405..135052633hg19UCSC Ensembl
Cytoband6q23.2
Allele length
AssemblyAllele length
hg381229
hg191229
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18139450
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6602316
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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