A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6421079



Internal ID21078632
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr7:141008733..141009201hg38UCSC Ensembl
chr7:140708533..140709001hg19UCSC Ensembl
Cytoband7q34
Allele length
AssemblyAllele length
hg38469
hg19469
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18150731
Samples
Known GenesMRPS33
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6421079
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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