A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6609063



Internal ID20982134
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr7:17821383..18325020hg38UCSC Ensembl
chr7:17861006..18364643hg19UCSC Ensembl
Cytoband7p21.1
Allele length
AssemblyAllele length
hg38503638
hg19503638
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18232298
Samples
Known GenesHDAC9, PRPS1L1, SNX13
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6609063
Frequency
Sample Size19652
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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