A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv18034716



Internal ID20601756
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr17:29750000..29769795hg38UCSC Ensembl
chr17:28077018..28096813hg19UCSC Ensembl
Cytoband17q11.2
Allele length
AssemblyAllele length
hg3819796
hg1919796
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6504253
Supporting Variants
Samples
Known GenesSSH2
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nssv18034716
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequency0


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