A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17122418



Internal ID21454621
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr5:16098767..16098767hg38UCSC Ensembl
chr5:16098876..16098876hg19UCSC Ensembl
Cytoband5p15.1
Allele length
AssemblyAllele length
hg38132
hg19132
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv5626547
Supporting Variants
SamplesHG02011
Known GenesMARCH11
MethodMerging
Analysis
PlatformSee merged experiments
Comments
ReferenceEbert_et_al_2021
Pubmed ID33632895
Accession Number(s)nssv17122418
Frequency
Sample Size35
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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