A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv18035689



Internal ID20602729
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr17:43144505..43149787hg38UCSC Ensembl
chr17:41296522..41301804hg19UCSC Ensembl
Cytoband17q21.31
Allele length
AssemblyAllele length
hg385283
hg195283
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6512917
Supporting Variants
Samples
Known GenesNBR2
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nssv18035689
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequency0


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