A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6415191



Internal ID21072744
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr6:62680666..62804762hg38UCSC Ensembl
chr6:63390571..63514667hg19UCSC Ensembl
Cytoband6q11.2
Allele length
AssemblyAllele length
hg38124097
hg19124097
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18145583
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6415191
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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