A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17071291



Internal ID21481176
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr10:75469289..75469289hg38UCSC Ensembl
chr10:77229047..77229047hg19UCSC Ensembl
Cytoband10q22.2
Allele length
AssemblyAllele length
hg38343
hg19343
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv5630798
Supporting Variants
SamplesHG03683
Known Genes
MethodMerging
Analysis
PlatformSee merged experiments
Comments
ReferenceEbert_et_al_2021
Pubmed ID33632895
Accession Number(s)nssv17071291
Frequency
Sample Size35
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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