A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6449153



Internal ID21106706
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr10:93709674..93713462hg38UCSC Ensembl
chr10:95469431..95473219hg19UCSC Ensembl
Cytoband10q23.33
Allele length
AssemblyAllele length
hg383789
hg193789
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17985214
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6449153
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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