A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17978293



Internal ID20545333
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr10:117015578..117018818hg38UCSC Ensembl
chr10:118775089..118778329hg19UCSC Ensembl
Cytoband10q25.3
Allele length
AssemblyAllele length
hg383241
hg193241
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6437886
Supporting Variants
Samples
Known GenesKIAA1598
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nssv17978293
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequency0


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