A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17978960



Internal ID20546000
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr10:17226142..17226420hg38UCSC Ensembl
chr10:17268141..17268419hg19UCSC Ensembl
Cytoband10p13
Allele length
AssemblyAllele length
hg38279
hg19279
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6449076
Supporting Variants
Samples
Known GenesVIM-AS1
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nssv17978960
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequency0.00015


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