A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv18151767



Internal ID20718807
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr7:135379101..135380100hg38UCSC Ensembl
chr7:135063853..135064852hg19UCSC Ensembl
Cytoband7q33
Allele length
AssemblyAllele length
hg381000
hg191000
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6434183
Supporting Variants
Samples
Known GenesCNOT4
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nssv18151767
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequency0


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