A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv3939967



Internal ID21360036
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr10:127502449..127502449hg38UCSC Ensembl
chr10:129300713..129300713hg19UCSC Ensembl
Cytoband10q26.2
Allele length
AssemblyAllele length
hg3897
hg1997
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv15190706
SamplesHG002
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceWenger_et_al_2019
Pubmed ID31406327
Accession Number(s)nsv3939967
Frequency
Sample Size1
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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