A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6417983



Internal ID21075536
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr9:13987324..14038327hg38UCSC Ensembl
chr9:13987323..14038326hg19UCSC Ensembl
Cytoband9p23
Allele length
AssemblyAllele length
hg3851004
hg1951004
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18174910
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6417983
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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