A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17120072



Internal ID21409781
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr4:38807765..38807765hg38UCSC Ensembl
chr4:38809386..38809386hg19UCSC Ensembl
Cytoband4p14
Allele length
AssemblyAllele length
hg3896
hg1996
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv5611382
Supporting Variants
SamplesHG00512
Known Genes
MethodMerging
Analysis
PlatformSee merged experiments
Comments
ReferenceEbert_et_al_2021
Pubmed ID33632895
Accession Number(s)nssv17120072
Frequency
Sample Size35
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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