A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv18218709



Internal ID20785749
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr6:35019815..35045188hg38UCSC Ensembl
chr6:34987592..35012965hg19UCSC Ensembl
Cytoband6p21.31
Allele length
AssemblyAllele length
hg3825374
hg1925374
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6395783
Supporting Variants
Samples
Known GenesANKS1A
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nssv18218709
Frequency
Sample Size19652
Observed Gain1
Observed Loss0
Observed Complex0
Frequency0


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