A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv18236493



Internal ID20803533
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr7:87871601..87876900hg38UCSC Ensembl
chr7:87500916..87506215hg19UCSC Ensembl
Cytoband7q21.12
Allele length
AssemblyAllele length
hg385300
hg195300
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6609852
Supporting Variants
Samples
Known GenesDBF4, SLC25A40
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nssv18236493
Frequency
Sample Size19652
Observed Gain1
Observed Loss0
Observed Complex0
Frequency0


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