A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5639810



Internal ID21588115
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr7:31938649..31938649hg38UCSC Ensembl
chr7:31978262..31978262hg19UCSC Ensembl
Cytoband7p14.3
Allele length
AssemblyAllele length
hg3868
hg1968
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17150832
SamplesHG00864
Known GenesPDE1C
MethodMerging
Analysis
PlatformSee merged experiments
Comments
ReferenceEbert_et_al_2021
Pubmed ID33632895
Accession Number(s)nsv5639810
Frequency
Sample Size35
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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