A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17129656



Internal ID21453772
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr5:14455468..14455584hg38UCSC Ensembl
chr5:14455577..14455693hg19UCSC Ensembl
Cytoband5p15.2
Allele length
AssemblyAllele length
hg38117
hg19117
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv5570918
Supporting Variants
SamplesHG02011
Known GenesTRIO
MethodMerging
Analysis
PlatformSee merged experiments
Comments
ReferenceEbert_et_al_2021
Pubmed ID33632895
Accession Number(s)nssv17129656
Frequency
Sample Size35
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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