A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv18151399



Internal ID20718439
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr7:155405363..155410561hg38UCSC Ensembl
chr7:155198058..155203256hg19UCSC Ensembl
Cytoband7q36.3
Allele length
AssemblyAllele length
hg385199
hg195199
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6427540
Supporting Variants
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nssv18151399
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequency0.00024


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