A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5666707



Internal ID21615013
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr20:57190356..57190356hg38UCSC Ensembl
chr20:55765412..55765412hg19UCSC Ensembl
Cytoband20q13.31
Allele length
AssemblyAllele length
hg3872
hg1972
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17116631
SamplesNA19239
Known GenesBMP7
MethodMerging
Analysis
PlatformSee merged experiments
Comments
ReferenceEbert_et_al_2021
Pubmed ID33632895
Accession Number(s)nsv5666707
Frequency
Sample Size35
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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