A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17983444



Internal ID20550484
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr10:76535603..76542445hg38UCSC Ensembl
chr10:78295361..78302203hg19UCSC Ensembl
Cytoband10q22.3
Allele length
AssemblyAllele length
hg386843
hg196843
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6438847
Supporting Variants
Samples
Known GenesC10orf11
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nssv17983444
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequency0.0001


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