A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17979550



Internal ID20546590
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr10:118320301..118320857hg38UCSC Ensembl
chr10:120079813..120080369hg19UCSC Ensembl
Cytoband10q26.11
Allele length
AssemblyAllele length
hg38557
hg19557
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6445224
Supporting Variants
Samples
Known GenesFAM204A
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nssv17979550
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequency0.00043


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