A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv18155529



Internal ID20722569
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr7:2531134..2535178hg38UCSC Ensembl
chr7:2570768..2574812hg19UCSC Ensembl
Cytoband7p22.3
Allele length
AssemblyAllele length
hg384045
hg194045
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6609994
Supporting Variants
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nssv18155529
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequency0


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