A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17069574



Internal ID21408618
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr10:21430486..21430486hg38UCSC Ensembl
chr10:21719415..21719415hg19UCSC Ensembl
Cytoband10p12.31
Allele length
AssemblyAllele length
hg3878
hg1978
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv5638837
Supporting Variants
SamplesHG00512
Known Genes
MethodMerging
Analysis
PlatformSee merged experiments
Comments
ReferenceEbert_et_al_2021
Pubmed ID33632895
Accession Number(s)nssv17069574
Frequency
Sample Size35
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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