A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17978834



Internal ID20545874
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr10:128105729..128108602hg38UCSC Ensembl
chr10:129903993..129906866hg19UCSC Ensembl
Cytoband10q26.2
Allele length
AssemblyAllele length
hg382874
hg192874
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6444946
Supporting Variants
Samples
Known GenesMKI67
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nssv17978834
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequency0


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