A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv18212709



Internal ID20779749
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr5:10681630..10682591hg38UCSC Ensembl
chr5:10681742..10682703hg19UCSC Ensembl
Cytoband5p15.2
Allele length
AssemblyAllele length
hg38962
hg19962
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6383623
Supporting Variants
Samples
Known GenesDAP
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nssv18212709
Frequency
Sample Size19652
Observed Gain1
Observed Loss0
Observed Complex0
Frequency0.00037


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