A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17982537



Internal ID20549577
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr10:5661390..5662583hg38UCSC Ensembl
chr10:5703353..5704546hg19UCSC Ensembl
Cytoband10p15.1
Allele length
AssemblyAllele length
hg381194
hg191194
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6445449
Supporting Variants
Samples
Known GenesASB13
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nssv17982537
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequency0


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