A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv18234067



Internal ID20801107
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr7:138476518..138477245hg38UCSC Ensembl
chr7:138161263..138161990hg19UCSC Ensembl
Cytoband7q33
Allele length
AssemblyAllele length
hg38728
hg19728
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6424385
Supporting Variants
Samples
Known GenesTRIM24
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nssv18234067
Frequency
Sample Size19652
Observed Gain1
Observed Loss0
Observed Complex0
Frequency0


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