A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5637649



Internal ID21585954
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr10:97900570..97900570hg38UCSC Ensembl
chr10:99660327..99660327hg19UCSC Ensembl
Cytoband10q24.2
Allele length
AssemblyAllele length
hg38389
hg19389
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17072070
SamplesHG00512
Known GenesCRTAC1
MethodMerging
Analysis
PlatformSee merged experiments
Comments
ReferenceEbert_et_al_2021
Pubmed ID33632895
Accession Number(s)nsv5637649
Frequency
Sample Size35
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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