A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17977883



Internal ID20544923
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr10:114525050..114530149hg38UCSC Ensembl
chr10:116284809..116289908hg19UCSC Ensembl
Cytoband10q25.3
Allele length
AssemblyAllele length
hg385100
hg195100
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6449350
Supporting Variants
Samples
Known GenesABLIM1
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nssv17977883
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequency0


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