A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5651663



Internal ID21599968
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr13:87492124..87492124hg38UCSC Ensembl
chr13:88144379..88144379hg19UCSC Ensembl
Cytoband13q31.2
Allele length
AssemblyAllele length
hg38146
hg19146
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17087483
SamplesHG00731
Known GenesMIR4500HG
MethodMerging
Analysis
PlatformSee merged experiments
Comments
ReferenceEbert_et_al_2021
Pubmed ID33632895
Accession Number(s)nsv5651663
Frequency
Sample Size35
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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