A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5628206



Internal ID21576511
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr10:97900573..97900573hg38UCSC Ensembl
chr10:99660330..99660330hg19UCSC Ensembl
Cytoband10q24.2
Allele length
AssemblyAllele length
hg38128
hg19128
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17072071
SamplesHG00731
Known GenesCRTAC1
MethodMerging
Analysis
PlatformSee merged experiments
Comments
ReferenceEbert_et_al_2021
Pubmed ID33632895
Accession Number(s)nsv5628206
Frequency
Sample Size35
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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