A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17152890



Internal ID21424593
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr7:155367171..155367248hg38UCSC Ensembl
chr7:155159866..155159943hg19UCSC Ensembl
Cytoband7q36.3
Allele length
AssemblyAllele length
hg3878
hg1978
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv5580170
Supporting Variants
SamplesHG00731
Known GenesBLACE
MethodMerging
Analysis
PlatformSee merged experiments
Comments
ReferenceEbert_et_al_2021
Pubmed ID33632895
Accession Number(s)nssv17152890
Frequency
Sample Size35
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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