A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv18154315



Internal ID20721355
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr7:136059901..136060311hg38UCSC Ensembl
chr7:135744649..135745059hg19UCSC Ensembl
Cytoband7q33
Allele length
AssemblyAllele length
hg38411
hg19411
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6435453
Supporting Variants
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nssv18154315
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequency0.00096


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