A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv18160697



Internal ID20727737
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr7:96052691..96053532hg38UCSC Ensembl
chr7:95682003..95682844hg19UCSC Ensembl
Cytoband7q21.3
Allele length
AssemblyAllele length
hg38842
hg19842
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6619422
Supporting Variants
Samples
Known GenesDYNC1I1
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nssv18160697
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequency0.0005


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