A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv18185877



Internal ID20752917
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr10:125648501..125655700hg38UCSC Ensembl
chr10:127337070..127344269hg19UCSC Ensembl
Cytoband10q26.13
Allele length
AssemblyAllele length
hg387200
hg197200
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6452102
Supporting Variants
Samples
Known GenesTEX36
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nssv18185877
Frequency
Sample Size19652
Observed Gain1
Observed Loss0
Observed Complex0
Frequency0


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