A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv18187417



Internal ID20754457
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr10:26582722..26640993hg38UCSC Ensembl
chr10:26871651..26929922hg19UCSC Ensembl
Cytoband10p12.1
Allele length
AssemblyAllele length
hg3858272
hg1958272
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6437653
Supporting Variants
Samples
Known GenesLINC00264
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nssv18187417
Frequency
Sample Size19652
Observed Gain1
Observed Loss0
Observed Complex0
Frequency0


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