A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv18234289



Internal ID20801329
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr6:89111826..89628748hg38UCSC Ensembl
chr6:89821545..90338467hg19UCSC Ensembl
Cytoband6q15
Allele length
AssemblyAllele length
hg38516923
hg19516923
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6413108
Supporting Variants
Samples
Known GenesANKRD6, GABRR1, GABRR2, PM20D2, RRAGD, SRSF12, UBE2J1
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nssv18234289
Frequency
Sample Size19652
Observed Gain1
Observed Loss0
Observed Complex0
Frequency0


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