A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6419879



Internal ID21077432
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr8:61125376..61138136hg38UCSC Ensembl
chr8:62037935..62050695hg19UCSC Ensembl
Cytoband8q12.2
Allele length
AssemblyAllele length
hg3812761
hg1912761
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18168705
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6419879
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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