A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17139439



Internal ID21418712
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr4:2960889..2960957hg38UCSC Ensembl
chr4:2962616..2962684hg19UCSC Ensembl
Cytoband4p16.3
Allele length
AssemblyAllele length
hg3869
hg1969
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv5580233
Supporting Variants
SamplesHG00731
Known GenesNOP14
MethodMerging
Analysis
PlatformSee merged experiments
Comments
ReferenceEbert_et_al_2021
Pubmed ID33632895
Accession Number(s)nssv17139439
Frequency
Sample Size35
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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