A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv3525091



Internal ID22394467
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr3:155125277..155125341hg38UCSC Ensembl
chr3:154843066..154843130hg19UCSC Ensembl
Cytoband3q25.2
Allele length
AssemblyAllele length
hg3865
hg1965
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv14308382, nssv14308381, nssv14308383
SamplesHG00512, HG00731, HG00732
Known GenesMME
MethodSequencing
AnalysisMultiple analysis algorthms
PlatformIllumina HiSeq
Comments
ReferenceChaisson_et_al_2019
Pubmed ID30992455
Accession Number(s)nsv3525091
Frequency
Sample Size9
Observed Gain0
Observed Loss3
Observed Complex0
Frequencyn/a


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