A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5640018



Internal ID21588323
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr10:24411281..24411281hg38UCSC Ensembl
chr10:24700210..24700210hg19UCSC Ensembl
Cytoband10p12.1
Allele length
AssemblyAllele length
hg38312
hg19312
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17068168
SamplesHG03125
Known GenesKIAA1217
MethodMerging
Analysis
PlatformSee merged experiments
Comments
ReferenceEbert_et_al_2021
Pubmed ID33632895
Accession Number(s)nsv5640018
Frequency
Sample Size35
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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