A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv18155560



Internal ID20722600
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr7:25939998..25942928hg38UCSC Ensembl
chr7:25979618..25982548hg19UCSC Ensembl
Cytoband7p15.2
Allele length
AssemblyAllele length
hg382931
hg192931
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6612164
Supporting Variants
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nssv18155560
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequency0.00254


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