A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv18154864



Internal ID20721904
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr7:22810289..22811439hg38UCSC Ensembl
chr7:22849908..22851058hg19UCSC Ensembl
Cytoband7p15.3
Allele length
AssemblyAllele length
hg381151
hg191151
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6616782
Supporting Variants
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nssv18154864
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequency0


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