A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17981286



Internal ID20548326
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr10:28273701..28283700hg38UCSC Ensembl
chr10:28562630..28572629hg19UCSC Ensembl
Cytoband10p12.1
Allele length
AssemblyAllele length
hg3810000
hg1910000
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6444516
Supporting Variants
Samples
Known GenesMPP7
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nssv17981286
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequency0.00341


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