A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6424385



Internal ID21081938
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 StatusM
Merged Variants
Supporting Variantsnssv18234067
Samples
Known GenesTRIM24
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6424385
Frequency
Sample Size19652
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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