A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6615067



Internal ID20988138
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr6:133899353..133903193hg38UCSC Ensembl
chr6:134220491..134224331hg19UCSC Ensembl
Cytoband6q23.2
Allele length
AssemblyAllele length
hg383841
hg193841
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18139402
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6615067
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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