A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv18035726



Internal ID20602766
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr17:43770401..43772200hg38UCSC Ensembl
chr17:41847769..41849568hg19UCSC Ensembl
Cytoband17q21.31
Allele length
AssemblyAllele length
hg381800
hg191800
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6512830
Supporting Variants
Samples
Known GenesDUSP3
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nssv18035726
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequency0


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