A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv18215509



Internal ID20782549
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr6:125735201..125820466hg38UCSC Ensembl
chr6:126056347..126141612hg19UCSC Ensembl
Cytoband6q22.31
Allele length
AssemblyAllele length
hg3885266
hg1985266
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6602879
Supporting Variants
Samples
Known GenesHEY2, NCOA7
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nssv18215509
Frequency
Sample Size19652
Observed Gain1
Observed Loss0
Observed Complex0
Frequency0


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