A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5647634



Internal ID21595939
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr11:10633692..10633692hg38UCSC Ensembl
chr11:10655239..10655239hg19UCSC Ensembl
Cytoband11p15.4
Allele length
AssemblyAllele length
hg382500
hg192500
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17072429
SamplesHG03732
Known GenesMRVI1
MethodMerging
Analysis
PlatformSee merged experiments
Comments
ReferenceEbert_et_al_2021
Pubmed ID33632895
Accession Number(s)nsv5647634
Frequency
Sample Size35
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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