A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6441797



Internal ID21099350
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr10:89745984..89747803hg38UCSC Ensembl
chr10:91505741..91507560hg19UCSC Ensembl
Cytoband10q23.31
Allele length
AssemblyAllele length
hg381820
hg191820
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17984971
Samples
Known GenesKIF20B
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6441797
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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