A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17152238



Internal ID21507169
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr8:73325952..73325952hg38UCSC Ensembl
chr8:74238187..74238187hg19UCSC Ensembl
Cytoband8q21.11
Allele length
AssemblyAllele length
hg3852
hg1952
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv5632612
Supporting Variants
SamplesNA19983
Known Genes
MethodMerging
Analysis
PlatformSee merged experiments
Comments
ReferenceEbert_et_al_2021
Pubmed ID33632895
Accession Number(s)nssv17152238
Frequency
Sample Size35
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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