A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17124578



Internal ID21442698
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr4:60875021..60875074hg38UCSC Ensembl
chr4:61740739..61740792hg19UCSC Ensembl
Cytoband4q13.1
Allele length
AssemblyAllele length
hg3854
hg1954
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv5564841
Supporting Variants
SamplesHG00732
Known Genes
MethodMerging
Analysis
PlatformSee merged experiments
Comments
ReferenceEbert_et_al_2021
Pubmed ID33632895
Accession Number(s)nssv17124578
Frequency
Sample Size35
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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