A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5656714



Internal ID21605019
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr16:88045162..88045162hg38UCSC Ensembl
chr16:88078768..88078768hg19UCSC Ensembl
Cytoband16q24.2
Allele length
AssemblyAllele length
hg3867
hg1967
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17088319
SamplesHG01114
Known GenesBANP
MethodMerging
Analysis
PlatformSee merged experiments
Comments
ReferenceEbert_et_al_2021
Pubmed ID33632895
Accession Number(s)nsv5656714
Frequency
Sample Size35
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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