A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17977740



Internal ID20544780
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr10:104269124..104282063hg38UCSC Ensembl
chr10:106028882..106041821hg19UCSC Ensembl
Cytoband10q25.1
Allele length
AssemblyAllele length
hg3812940
hg1912940
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6439159
Supporting Variants
Samples
Known GenesGSTO2
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nssv17977740
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequency0


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