A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17131509



Internal ID21446847
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr4:38880090..38880144hg38UCSC Ensembl
chr4:38881711..38881765hg19UCSC Ensembl
Cytoband4p14
Allele length
AssemblyAllele length
hg3855
hg1955
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv5565882
Supporting Variants
SamplesHG00732
Known GenesFAM114A1
MethodMerging
Analysis
PlatformSee merged experiments
Comments
ReferenceEbert_et_al_2021
Pubmed ID33632895
Accession Number(s)nssv17131509
Frequency
Sample Size35
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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