A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5633040



Internal ID21581345
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr7:99507523..99507523hg38UCSC Ensembl
chr7:99105146..99105146hg19UCSC Ensembl
Cytoband7q22.1
Allele length
AssemblyAllele length
hg3868
hg1968
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17143492
SamplesHG02011
Known GenesZKSCAN5
MethodMerging
Analysis
PlatformSee merged experiments
Comments
ReferenceEbert_et_al_2021
Pubmed ID33632895
Accession Number(s)nsv5633040
Frequency
Sample Size35
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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