A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6609217



Internal ID20982288
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr6:115382797..115397195hg38UCSC Ensembl
chr6:115703961..115718359hg19UCSC Ensembl
Cytoband6q22.1
Allele length
AssemblyAllele length
hg3814399
hg1914399
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18138176
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6609217
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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