A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17984080



Internal ID20551120
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr10:75830461..75830603hg38UCSC Ensembl
chr10:77590219..77590361hg19UCSC Ensembl
Cytoband10q22.2
Allele length
AssemblyAllele length
hg38143
hg19143
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6448767
Supporting Variants
Samples
Known GenesC10orf11
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nssv17984080
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequency0


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