A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv18179214



Internal ID20746254
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr10:124848627..125027555hg38UCSC Ensembl
chr10:126537196..126716124hg19UCSC Ensembl
Cytoband10q26.13
Allele length
AssemblyAllele length
hg38178929
hg19178929
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6440618
Supporting Variants
Samples
Known GenesCTBP2, ZRANB1
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nssv18179214
Frequency
Sample Size19652
Observed Gain1
Observed Loss0
Observed Complex0
Frequency0


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