A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv3519865



Internal ID22389272
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr4:40233406..40235439hg38UCSC Ensembl
chr4:40235026..40237059hg19UCSC Ensembl
Cytoband4p14
Allele length
AssemblyAllele length
hg382034
hg192034
Variant TypeOTHER complex
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv14313005, nssv14313004, nssv14313007, nssv14313006, nssv14313003
SamplesNA19238, NA19239, HG00731, NA19240, HG00733
Known GenesRHOH
MethodSequencing
AnalysisMultiple analysis algorthms
PlatformIllumina HiSeq
Commentscomplex variant
ReferenceChaisson_et_al_2019
Pubmed ID30992455
Accession Number(s)nsv3519865
Frequency
Sample Size9
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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