A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17983878



Internal ID20550918
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr10:73900884..73947465hg38UCSC Ensembl
chr10:75660642..75707223hg19UCSC Ensembl
Cytoband10q22.2
Allele length
AssemblyAllele length
hg3846582
hg1946582
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6438177
Supporting Variants
Samples
Known GenesC10orf55, PLAU
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nssv17983878
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequency0


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