A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6605440



Internal ID20978511
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr6:144684064..144786301hg38UCSC Ensembl
chr6:145005200..145107437hg19UCSC Ensembl
Cytoband6q24.2
Allele length
AssemblyAllele length
hg38102238
hg19102238
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18216935
Samples
Known GenesUTRN
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6605440
Frequency
Sample Size19652
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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