A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17977258



Internal ID20544299
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr10:102349049..102349416hg38UCSC Ensembl
chr10:104108806..104109173hg19UCSC Ensembl
Cytoband10q24.32
Allele length
AssemblyAllele length
hg38368
hg19368
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6442518
Supporting Variants
Samples
Known GenesGBF1
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nssv17977258
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequency0.00057


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