A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17979251



Internal ID20546291
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr10:24315940..24316481hg38UCSC Ensembl
chr10:24604869..24605410hg19UCSC Ensembl
Cytoband10p12.1
Allele length
AssemblyAllele length
hg38542
hg19542
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6438662
Supporting Variants
Samples
Known GenesKIAA1217
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nssv17979251
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequency0.00104


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