A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6606790



Internal ID20979861
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr6:140450448..140494929hg38UCSC Ensembl
chr6:140771585..140816066hg19UCSC Ensembl
Cytoband6q24.1
Allele length
AssemblyAllele length
hg3844482
hg1944482
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv6427n223
Supporting Variantsnssv18138569
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6606790
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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