A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17071755



Internal ID21445818
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr10:88132299..88132299hg38UCSC Ensembl
chr10:89892056..89892056hg19UCSC Ensembl
Cytoband10q23.31
Allele length
AssemblyAllele length
hg3896
hg1996
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv5633820
Supporting Variants
SamplesHG00732
Known Genes
MethodMerging
Analysis
PlatformSee merged experiments
Comments
ReferenceEbert_et_al_2021
Pubmed ID33632895
Accession Number(s)nssv17071755
Frequency
Sample Size35
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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