A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv18154860



Internal ID20721900
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr7:22769359..22773962hg38UCSC Ensembl
chr7:22808978..22813581hg19UCSC Ensembl
Cytoband7p15.3
Allele length
AssemblyAllele length
hg384604
hg194604
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6618922
Supporting Variants
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nssv18154860
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequency0


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