A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv18035236



Internal ID20602276
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr17:37472893..37516077hg38UCSC Ensembl
chr17:35832997..35876180hg19UCSC Ensembl
Cytoband17q12
Allele length
AssemblyAllele length
hg3843185
hg1943184
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6501563
Supporting Variants
Samples
Known GenesDUSP14, SYNRG, TADA2A
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nssv18035236
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequency0


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