A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv18188150



Internal ID20755190
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr10:101136430..101167629hg38UCSC Ensembl
chr10:102896187..102927386hg19UCSC Ensembl
Cytoband10q24.31
Allele length
AssemblyAllele length
hg3831200
hg1931200
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6450689
Supporting Variants
Samples
Known GenesTLX1
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nssv18188150
Frequency
Sample Size19652
Observed Gain1
Observed Loss0
Observed Complex0
Frequency0


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