A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17131576



Internal ID21471626
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr4:183433679..183433679hg38UCSC Ensembl
chr4:184354832..184354832hg19UCSC Ensembl
Cytoband4q35.1
Allele length
AssemblyAllele length
hg3878
hg1978
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv5631354
Supporting Variants
SamplesHG03125
Known Genes
MethodMerging
Analysis
PlatformSee merged experiments
Comments
ReferenceEbert_et_al_2021
Pubmed ID33632895
Accession Number(s)nssv17131576
Frequency
Sample Size35
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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