A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5657527



Internal ID21605832
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr16:88077037..88077037hg38UCSC Ensembl
chr16:88110643..88110643hg19UCSC Ensembl
Cytoband16q24.2
Allele length
AssemblyAllele length
hg3880
hg1980
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17093088
SamplesHG00512
Known GenesBANP
MethodMerging
Analysis
PlatformSee merged experiments
Comments
ReferenceEbert_et_al_2021
Pubmed ID33632895
Accession Number(s)nsv5657527
Frequency
Sample Size35
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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