A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6430974



Internal ID21088527
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr8:61169226..61172011hg38UCSC Ensembl
chr8:62081785..62084570hg19UCSC Ensembl
Cytoband8q12.2
Allele length
AssemblyAllele length
hg382786
hg192786
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18168708
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6430974
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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