A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6430684



Internal ID21088237
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr9:32025501..32026600hg38UCSC Ensembl
chr9:32025499..32026598hg19UCSC Ensembl
Cytoband9p21.1
Allele length
AssemblyAllele length
hg381100
hg191100
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18195717
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6430684
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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