A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17983032



Internal ID20550072
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr10:68570268..68571622hg38UCSC Ensembl
chr10:70330025..70331379hg19UCSC Ensembl
Cytoband10q21.3
Allele length
AssemblyAllele length
hg381355
hg191355
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6439790
Supporting Variants
Samples
Known GenesTET1
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nssv17983032
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequency0.00157


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