A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6424437



Internal ID21081990
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr7:128954292..128954622hg38UCSC Ensembl
chr7:128594346..128594676hg19UCSC Ensembl
Cytoband7q32.1
Allele length
AssemblyAllele length
hg38331
hg19331
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18153332
Samples
Known GenesTNPO3
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6424437
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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