A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5634583



Internal ID21582888
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr7:36698050..36698050hg38UCSC Ensembl
chr7:36737655..36737655hg19UCSC Ensembl
Cytoband7p14.2
Allele length
AssemblyAllele length
hg38360
hg19360
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17146548
SamplesHG02818
Known GenesAOAH
MethodMerging
Analysis
PlatformSee merged experiments
Comments
ReferenceEbert_et_al_2021
Pubmed ID33632895
Accession Number(s)nsv5634583
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