A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6405795



Internal ID21063348
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr6:35665521..35677288hg38UCSC Ensembl
chr6:35633298..35645065hg19UCSC Ensembl
Cytoband6p21.31
Allele length
AssemblyAllele length
hg3811768
hg1911768
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18141721
Samples
Known GenesFKBP5
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6405795
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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