A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6446772



Internal ID21104325
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr10:102290795..102294628hg38UCSC Ensembl
chr10:104050552..104054385hg19UCSC Ensembl
Cytoband10q24.32
Allele length
AssemblyAllele length
hg383834
hg193834
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17977256
Samples
Known GenesGBF1
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6446772
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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