A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17141864



Internal ID21507715
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr8:37150231..37150231hg38UCSC Ensembl
chr8:37007749..37007749hg19UCSC Ensembl
Cytoband8p11.23
Allele length
AssemblyAllele length
hg38150
hg19150
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv5627223
Supporting Variants
SamplesNA20509
Known Genes
MethodMerging
Analysis
PlatformSee merged experiments
Comments
ReferenceEbert_et_al_2021
Pubmed ID33632895
Accession Number(s)nssv17141864
Frequency
Sample Size35
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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