A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv3937540



Internal ID21357610
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr10:33095433..33095433hg38UCSC Ensembl
chr10:33384361..33384361hg19UCSC Ensembl
Cytoband10p11.22
Allele length
AssemblyAllele length
hg38106
hg19106
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv15191604
SamplesHG002
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceWenger_et_al_2019
Pubmed ID31406327
Accession Number(s)nsv3937540
Frequency
Sample Size1
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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