A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv3930419



Internal ID21350489
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr6:117459392..117459490hg38UCSC Ensembl
chr6:117780555..117780653hg19UCSC Ensembl
Cytoband6q22.1
Allele length
AssemblyAllele length
hg3899
hg1999
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv15197702
SamplesHG002
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceWenger_et_al_2019
Pubmed ID31406327
Accession Number(s)nsv3930419
Frequency
Sample Size1
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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