A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17984434



Internal ID20551474
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr10:85706536..85709885hg38UCSC Ensembl
chr10:87466293..87469642hg19UCSC Ensembl
Cytoband10q23.1
Allele length
AssemblyAllele length
hg383350
hg193350
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6452308
Supporting Variants
Samples
Known GenesGRID1
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nssv17984434
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequency0


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