A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv18191772



Internal ID20758812
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr17:8047502..8080574hg38UCSC Ensembl
chr17:7950820..7983892hg19UCSC Ensembl
Cytoband17p13.1
Allele length
AssemblyAllele length
hg3833073
hg1933073
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6508964
Supporting Variants
Samples
Known GenesALOX12B, ALOX15B
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nssv18191772
Frequency
Sample Size19652
Observed Gain1
Observed Loss0
Observed Complex0
Frequency0


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