A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6431071



Internal ID21088624
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr9:31108297..32130239hg38UCSC Ensembl
chr9:31108295..32130237hg19UCSC Ensembl
Cytoband9p21.1
Allele length
AssemblyAllele length
hg381021943
hg191021943
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18195718
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6431071
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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