A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6419717



Internal ID21077270
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr7:129027494..129035166hg38UCSC Ensembl
chr7:128667548..128675220hg19UCSC Ensembl
Cytoband7q32.1
Allele length
AssemblyAllele length
hg387673
hg197673
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18153335
Samples
Known GenesTNPO3
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6419717
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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