A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv18182745



Internal ID20749785
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr10:6973550..7162777hg38UCSC Ensembl
chr10:7015512..7204739hg19UCSC Ensembl
Cytoband10p14
Allele length
AssemblyAllele length
hg38189228
hg19189228
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6450720
Supporting Variants
Samples
Known GenesSFMBT2
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nssv18182745
Frequency
Sample Size19652
Observed Gain1
Observed Loss0
Observed Complex0
Frequency0


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