A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17980170



Internal ID20547210
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr10:4215421..4217367hg38UCSC Ensembl
chr10:4257613..4259559hg19UCSC Ensembl
Cytoband10p15.1
Allele length
AssemblyAllele length
hg381947
hg191947
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6448737
Supporting Variants
Samples
Known GenesLINC00702
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nssv17980170
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequency0


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