A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv3938623



Internal ID21358694
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr11:76619300..76619300hg38UCSC Ensembl
chr11:76330344..76330344hg19UCSC Ensembl
Cytoband11q13.5
Allele length
AssemblyAllele length
hg38607
hg19607
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv15190927, nssv15190926
SamplesHG002
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceWenger_et_al_2019
Pubmed ID31406327
Accession Number(s)nsv3938623
Frequency
Sample Size1
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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