A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv3934568



Internal ID21354637
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr6:139307965..139308015hg38UCSC Ensembl
chr6:139629102..139629152hg19UCSC Ensembl
Cytoband6q24.1
Allele length
AssemblyAllele length
hg3851
hg1951
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv15197694
SamplesHG002
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceWenger_et_al_2019
Pubmed ID31406327
Accession Number(s)nsv3934568
Frequency
Sample Size1
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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