A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17981062



Internal ID20548102
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr10:19029870..19056643hg38UCSC Ensembl
chr10:19318799..19345572hg19UCSC Ensembl
Cytoband10p12.31
Allele length
AssemblyAllele length
hg3826774
hg1926774
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6435705
Supporting Variants
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nssv17981062
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequency0.00023


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