A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv18157976



Internal ID20725016
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr7:66094299..66096378hg38UCSC Ensembl
chr7:65559286..65561365hg19UCSC Ensembl
Cytoband7q11.21
Allele length
AssemblyAllele length
hg382080
hg192080
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6616445
Supporting Variants
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nssv18157976
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequency0


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