A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv3938643



Internal ID21358714
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr10:71296938..71296987hg38UCSC Ensembl
chr10:73056695..73056744hg19UCSC Ensembl
Cytoband10q22.1
Allele length
AssemblyAllele length
hg3850
hg1950
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv15181527
SamplesHG002
Known GenesUNC5B
MethodSequencing
Analysis
Platform
Comments
ReferenceWenger_et_al_2019
Pubmed ID31406327
Accession Number(s)nsv3938643
Frequency
Sample Size1
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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