A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv3525660



Internal ID22395038
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr3:97781298..97781351hg38UCSC Ensembl
chr3:97500142..97500195hg19UCSC Ensembl
Cytoband3q11.2
Allele length
AssemblyAllele length
hg3854
hg1954
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv14308907, nssv14308908
SamplesHG00731, HG00733
Known GenesARL6
MethodSequencing
AnalysisMultiple analysis algorthms
PlatformIllumina HiSeq
Comments
ReferenceChaisson_et_al_2019
Pubmed ID30992455
Accession Number(s)nsv3525660
Frequency
Sample Size9
Observed Gain0
Observed Loss2
Observed Complex0
Frequencyn/a


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