A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5655297



Internal ID21603602
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr12:30933300..30933300hg38UCSC Ensembl
chr12:31086234..31086234hg19UCSC Ensembl
Cytoband12p11.21
Allele length
AssemblyAllele length
hg3899
hg1999
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17079195
SamplesHG00732
Known GenesTSPAN11
MethodMerging
Analysis
PlatformSee merged experiments
Comments
ReferenceEbert_et_al_2021
Pubmed ID33632895
Accession Number(s)nsv5655297
Frequency
Sample Size35
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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