A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17141969



Internal ID21454320
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr8:143015720..143015720hg38UCSC Ensembl
chr8:144097137..144097137hg19UCSC Ensembl
Cytoband8q24.3
Allele length
AssemblyAllele length
hg3890
hg1990
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv5626101
Supporting Variants
SamplesHG02011
Known GenesLOC100133669
MethodMerging
Analysis
PlatformSee merged experiments
Comments
ReferenceEbert_et_al_2021
Pubmed ID33632895
Accession Number(s)nssv17141969
Frequency
Sample Size35
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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