A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6508324



Internal ID20881623
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr17:19950004..19955040hg38UCSC Ensembl
chr17:19853317..19858353hg19UCSC Ensembl
Cytoband17p11.2
Allele length
AssemblyAllele length
hg385037
hg195037
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18195911
Samples
Known GenesAKAP10
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6508324
Frequency
Sample Size19652
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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