A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17155842



Internal ID21413660
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr5:9512781..9514371hg38UCSC Ensembl
chr5:9512893..9514483hg19UCSC Ensembl
Cytoband5p15.31
Allele length
AssemblyAllele length
hg381591
hg191591
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv5567945
Supporting Variants
SamplesHG00513
Known GenesSEMA5A
MethodMerging
Analysis
PlatformSee merged experiments
Comments
ReferenceEbert_et_al_2021
Pubmed ID33632895
Accession Number(s)nssv17155842
Frequency
Sample Size35
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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