A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv3938281



Internal ID21358350
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr10:69409867..69409919hg38UCSC Ensembl
chr10:71169623..71169675hg19UCSC Ensembl
Cytoband10q22.1
Allele length
AssemblyAllele length
hg3853
hg1953
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv6n167
Supporting Variantsnssv15180852
SamplesHG002
Known GenesTACR2
MethodSequencing
Analysis
Platform
Comments
ReferenceWenger_et_al_2019
Pubmed ID31406327
Accession Number(s)nsv3938281
Frequency
Sample Size1
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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