A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17985752



Internal ID20552792
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr10:97560912..97561770hg38UCSC Ensembl
chr10:99320669..99321527hg19UCSC Ensembl
Cytoband10q24.2
Allele length
AssemblyAllele length
hg38859
hg19859
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6447377
Supporting Variants
Samples
Known GenesUBTD1
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nssv17985752
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequency0.0025


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