A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17157024



Internal ID21466308
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr8:39822506..39822506hg38UCSC Ensembl
chr8:39680025..39680025hg19UCSC Ensembl
Cytoband8p11.22
Allele length
AssemblyAllele length
hg38327
hg19327
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv5625935
Supporting Variants
SamplesHG03065
Known GenesADAM2
MethodMerging
Analysis
PlatformSee merged experiments
Comments
ReferenceEbert_et_al_2021
Pubmed ID33632895
Accession Number(s)nssv17157024
Frequency
Sample Size35
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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