A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6603857



Internal ID20976928
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr6:139534758..139541621hg38UCSC Ensembl
chr6:139855895..139862758hg19UCSC Ensembl
Cytoband6q24.1
Allele length
AssemblyAllele length
hg386864
hg196864
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18138491
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6603857
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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