A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv18161429



Internal ID20728469
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr7:90349801..90351800hg38UCSC Ensembl
chr7:89979115..89981114hg19UCSC Ensembl
Cytoband7q21.13
Allele length
AssemblyAllele length
hg382000
hg192000
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6603284
Supporting Variants
Samples
Known GenesGTPBP10
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nssv18161429
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequency0


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