A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6443905



Internal ID21101458
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr10:102288510..102307564hg38UCSC Ensembl
chr10:104048267..104067321hg19UCSC Ensembl
Cytoband10q24.32
Allele length
AssemblyAllele length
hg3819055
hg1919055
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17977255
Samples
Known GenesGBF1
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6443905
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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