A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17979551



Internal ID20546591
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr10:118321860..118325315hg38UCSC Ensembl
chr10:120081372..120084827hg19UCSC Ensembl
Cytoband10q26.11
Allele length
AssemblyAllele length
hg383456
hg193456
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6439663
Supporting Variants
Samples
Known GenesFAM204A
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nssv17979551
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequency0


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