A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5633026



Internal ID21581331
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr10:70554970..70554970hg38UCSC Ensembl
chr10:72314726..72314726hg19UCSC Ensembl
Cytoband10q22.1
Allele length
AssemblyAllele length
hg38218
hg19218
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17071612, nssv17071613
SamplesHG00731, NA20847
Known GenesPALD1
MethodMerging
Analysis
PlatformSee merged experiments
Comments
ReferenceEbert_et_al_2021
Pubmed ID33632895
Accession Number(s)nsv5633026
Frequency
Sample Size35
Observed Gain2
Observed Loss0
Observed Complex0
Frequencyn/a


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