A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5628875



Internal ID21577180
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr7:121395234..121395234hg38UCSC Ensembl
chr7:121035288..121035288hg19UCSC Ensembl
Cytoband7q31.31
Allele length
AssemblyAllele length
hg3854
hg1954
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17151208
SamplesNA19983
Known GenesFAM3C
MethodMerging
Analysis
PlatformSee merged experiments
Comments
ReferenceEbert_et_al_2021
Pubmed ID33632895
Accession Number(s)nsv5628875
Frequency
Sample Size35
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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