A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17126470



Internal ID21401202
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr4:182970952..182970952hg38UCSC Ensembl
chr4:183892105..183892105hg19UCSC Ensembl
Cytoband4q35.1
Allele length
AssemblyAllele length
hg3893
hg1993
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv5636959
Supporting Variants
SamplesHG00096
Known Genes
MethodMerging
Analysis
PlatformSee merged experiments
Comments
ReferenceEbert_et_al_2021
Pubmed ID33632895
Accession Number(s)nssv17126470
Frequency
Sample Size35
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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