A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6428313



Internal ID21085866
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr9:12021986..12104577hg38UCSC Ensembl
chr9:12021986..12104577hg19UCSC Ensembl
Cytoband9p23
Allele length
AssemblyAllele length
hg3882592
hg1982592
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv7609n223
Supporting Variantsnssv18174246
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6428313
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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