A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6448094



Internal ID21105647
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr10:26443911..26448152hg38UCSC Ensembl
chr10:26732840..26737081hg19UCSC Ensembl
Cytoband10p12.1
Allele length
AssemblyAllele length
hg384242
hg194242
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17981168
Samples
Known GenesAPBB1IP
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6448094
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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