A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv3245610



Internal ID22376196
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr7:137187146..137210316hg38UCSC Ensembl
chr7:136871893..136895063hg19UCSC Ensembl
Cytoband7q33
Allele length
AssemblyAllele length
hg3823171
hg1923171
Variant TypeOTHER inversion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv14339093, nssv14339094
SamplesNA19238, NA19240
Known Genes
MethodSequencing
AnalysisMultiple analysis algorthms
PlatformIllumina HiSeq
Comments
ReferenceChaisson_et_al_2019
Pubmed ID30992455
Accession Number(s)nsv3245610
Frequency
Sample Size9
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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