A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv3534699



Internal ID22403975
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr7:886113..886113hg38UCSC Ensembl
chr7:925750..925750hg19UCSC Ensembl
Cytoband7p22.3
Allele length
AssemblyAllele length
hg3815615
hg1915615
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv14427122, nssv14401275
SamplesNA19240, HG00514
Known GenesGET4
MethodMerging
AnalysisPhasedSV,MsPAC, Multiple Illumina callers, BioNano Genomics software
PlatformSee merged experiments
Comments
ReferenceChaisson_et_al_2019
Pubmed ID30992455
Accession Number(s)nsv3534699
Frequency
Sample Size9
Observed Gain2
Observed Loss0
Observed Complex0
Frequencyn/a


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