A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5643347



Internal ID21591652
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr7:39792014..39792014hg38UCSC Ensembl
chr7:39831613..39831613hg19UCSC Ensembl
Cytoband7p14.1
Allele length
AssemblyAllele length
hg382771
hg192771
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17156858
SamplesHG03732
Known GenesLINC00265
MethodMerging
Analysis
PlatformSee merged experiments
Comments
ReferenceEbert_et_al_2021
Pubmed ID33632895
Accession Number(s)nsv5643347
Frequency
Sample Size35
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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