A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5666872



Internal ID21615179
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr21:38207570..38207570hg38UCSC Ensembl
chr21:39579664..39579664hg19UCSC Ensembl
Cytoband21q22.13
Allele length
AssemblyAllele length
hg3883
hg1983
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17118933
SamplesHG00731
Known GenesDSCR10
MethodMerging
Analysis
PlatformSee merged experiments
Comments
ReferenceEbert_et_al_2021
Pubmed ID33632895
Accession Number(s)nsv5666872
Frequency
Sample Size35
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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