A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17984982



Internal ID20552022
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr10:8982006..8989205hg38UCSC Ensembl
chr10:9023969..9031168hg19UCSC Ensembl
Cytoband10p14
Allele length
AssemblyAllele length
hg387200
hg197200
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6454573
Supporting Variants
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nssv17984982
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequency0


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