A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv3939265



Internal ID21359334
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr10:47918377..47918423hg38UCSC Ensembl
chr10:47083158..47083218hg19UCSC Ensembl
Cytoband10q11.22
Allele length
AssemblyAllele length
hg3847
hg1961
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv15180824
SamplesHG002
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceWenger_et_al_2019
Pubmed ID31406327
Accession Number(s)nsv3939265
Frequency
Sample Size1
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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