A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv18151006



Internal ID20718046
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr7:133088348..133105722hg38UCSC Ensembl
chr7:132773108..132790482hg19UCSC Ensembl
Cytoband7q33
Allele length
AssemblyAllele length
hg3817375
hg1917375
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6425717
Supporting Variants
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nssv18151006
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequency0.00013


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