A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5629537



Internal ID21577842
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr8:133213962..133213962hg38UCSC Ensembl
chr8:134226205..134226205hg19UCSC Ensembl
Cytoband8q24.22
Allele length
AssemblyAllele length
hg38232
hg19232
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17147565
SamplesHG01114
Known GenesWISP1
MethodMerging
Analysis
PlatformSee merged experiments
Comments
ReferenceEbert_et_al_2021
Pubmed ID33632895
Accession Number(s)nsv5629537
Frequency
Sample Size35
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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