A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv18155022



Internal ID20722062
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr7:24627118..24639814hg38UCSC Ensembl
chr7:24666737..24679433hg19UCSC Ensembl
Cytoband7p15.3
Allele length
AssemblyAllele length
hg3812697
hg1912697
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6607484
Supporting Variants
Samples
Known GenesMPP6
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nssv18155022
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequency0


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