A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17981390



Internal ID20548430
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr10:30281271..30285680hg38UCSC Ensembl
chr10:30570200..30574609hg19UCSC Ensembl
Cytoband10p11.23
Allele length
AssemblyAllele length
hg384410
hg194410
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6453668
Supporting Variants
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nssv17981390
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequency0


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