A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv18229093



Internal ID20796133
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr7:139446604..139469707hg38UCSC Ensembl
chr7:139131350..139154453hg19UCSC Ensembl
Cytoband7q34
Allele length
AssemblyAllele length
hg3823104
hg1923104
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6429378
Supporting Variants
Samples
Known GenesKLRG2
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nssv18229093
Frequency
Sample Size19652
Observed Gain1
Observed Loss0
Observed Complex0
Frequency0


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