A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6452037



Internal ID21109590
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr9:93430975..93437677hg38UCSC Ensembl
chr9:96193257..96199959hg19UCSC Ensembl
Cytoband9q22.31
Allele length
AssemblyAllele length
hg386703
hg196703
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18195020
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6452037
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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