A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv18155002



Internal ID20722042
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr7:24430301..24433300hg38UCSC Ensembl
chr7:24469920..24472919hg19UCSC Ensembl
Cytoband7p15.3
Allele length
AssemblyAllele length
hg383000
hg193000
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6609229
Supporting Variants
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nssv18155002
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequency0


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