A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv18195918



Internal ID20762958
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr10:110123336..110154939hg38UCSC Ensembl
chr10:111883094..111914697hg19UCSC Ensembl
Cytoband10q25.1
Allele length
AssemblyAllele length
hg3831604
hg1931604
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6441997
Supporting Variants
Samples
Known GenesADD3
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nssv18195918
Frequency
Sample Size19652
Observed Gain1
Observed Loss0
Observed Complex0
Frequency0


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