A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6436563



Internal ID21094116
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr10:102556656..102556963hg38UCSC Ensembl
chr10:104316413..104316720hg19UCSC Ensembl
Cytoband10q24.32
Allele length
AssemblyAllele length
hg38308
hg19308
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17977267
Samples
Known GenesSUFU
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6436563
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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