A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17128942



Internal ID21416519
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr4:36468282..36468614hg38UCSC Ensembl
chr4:36469904..36470236hg19UCSC Ensembl
Cytoband4p14
Allele length
AssemblyAllele length
hg38333
hg19333
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv5570778
Supporting Variants
SamplesHG00731
Known Genes
MethodMerging
Analysis
PlatformSee merged experiments
Comments
ReferenceEbert_et_al_2021
Pubmed ID33632895
Accession Number(s)nssv17128942
Frequency
Sample Size35
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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