A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17979499



Internal ID20546539
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr10:110304401..110304800hg38UCSC Ensembl
chr10:112064159..112064558hg19UCSC Ensembl
Cytoband10q25.2
Allele length
AssemblyAllele length
hg38400
hg19400
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6449009
Supporting Variants
Samples
Known GenesSMNDC1
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nssv17979499
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequency0.01409


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