A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5656920



Internal ID21605225
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr11:1584674..1584674hg38UCSC Ensembl
chr11:1605904..1605904hg19UCSC Ensembl
Cytoband11p15.5
Allele length
AssemblyAllele length
hg3860
hg1960
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17073741
SamplesHG00731
Known GenesKRTAP5-1, KRTAP5-AS1, MOB2
MethodMerging
Analysis
PlatformSee merged experiments
Comments
ReferenceEbert_et_al_2021
Pubmed ID33632895
Accession Number(s)nsv5656920
Frequency
Sample Size35
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


Hosted by The Centre for Applied Genomics
Grant support for DGV
Please read the usage disclaimer