A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv3237847



Internal ID22373987
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr7:23587020..23678599hg38UCSC Ensembl
chr7:23626639..23718218hg19UCSC Ensembl
Cytoband7p15.3
Allele length
AssemblyAllele length
hg3891580
hg1991580
Variant TypeOTHER inversion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv14333086
SamplesNA19238
Known GenesCCDC126
MethodSequencing
AnalysisMultiple analysis algorthms
PlatformIllumina HiSeq
Comments
ReferenceChaisson_et_al_2019
Pubmed ID30992455
Accession Number(s)nsv3237847
Frequency
Sample Size9
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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