A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6444014



Internal ID21101567
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr10:71212101..71213700hg38UCSC Ensembl
chr10:72971858..72973457hg19UCSC Ensembl
Cytoband10q22.1
Allele length
AssemblyAllele length
hg381600
hg191600
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18187853
Samples
Known GenesUNC5B
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6444014
Frequency
Sample Size19652
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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