A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17070460



Internal ID21412421
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr10:62947532..62947532hg38UCSC Ensembl
chr10:64707292..64707292hg19UCSC Ensembl
Cytoband10q21.3
Allele length
AssemblyAllele length
hg3880
hg1980
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv5626603
Supporting Variants
SamplesHG00513
Known Genes
MethodMerging
Analysis
PlatformSee merged experiments
Comments
ReferenceEbert_et_al_2021
Pubmed ID33632895
Accession Number(s)nssv17070460
Frequency
Sample Size35
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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