A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv18161440



Internal ID20728480
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr7:90472515..90522394hg38UCSC Ensembl
chr7:90101829..90151708hg19UCSC Ensembl
Cytoband7q21.13
Allele length
AssemblyAllele length
hg3849880
hg1949880
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6609372
Supporting Variants
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nssv18161440
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequency0


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