A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5639969



Internal ID21588274
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr7:32965879..32965879hg38UCSC Ensembl
chr7:33005491..33005491hg19UCSC Ensembl
Cytoband7p14.3
Allele length
AssemblyAllele length
hg3878
hg1978
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17153314
SamplesHG00733
Known GenesFKBP9
MethodMerging
Analysis
PlatformSee merged experiments
Comments
ReferenceEbert_et_al_2021
Pubmed ID33632895
Accession Number(s)nsv5639969
Frequency
Sample Size35
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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