A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6614492



Internal ID20987563
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr6:140806793..141420876hg38UCSC Ensembl
chr6:141127930..141742013hg19UCSC Ensembl
Cytoband6q24.1
Allele length
AssemblyAllele length
hg38614084
hg19614084
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18216896
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6614492
Frequency
Sample Size19652
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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