A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6607461



Internal ID20980532
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr6:132862857..132868247hg38UCSC Ensembl
chr6:133183996..133189386hg19UCSC Ensembl
Cytoband6q23.2
Allele length
AssemblyAllele length
hg385391
hg195391
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18140319
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6607461
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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