A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv18035233



Internal ID20602273
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr17:37418301..37421200hg38UCSC Ensembl
chr17:35778386..35781283hg19UCSC Ensembl
Cytoband17q12
Allele length
AssemblyAllele length
hg382900
hg192898
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6503756
Supporting Variants
Samples
Known GenesTADA2A
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nssv18035233
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequency0.03545


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