A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17070251



Internal ID21499187
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr10:4149430..4149430hg38UCSC Ensembl
chr10:4191622..4191622hg19UCSC Ensembl
Cytoband10p15.1
Allele length
AssemblyAllele length
hg3878
hg1978
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv5644129
Supporting Variants
SamplesNA19239
Known Genes
MethodMerging
Analysis
PlatformSee merged experiments
Comments
ReferenceEbert_et_al_2021
Pubmed ID33632895
Accession Number(s)nssv17070251
Frequency
Sample Size35
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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