A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv3526903



Internal ID22396287
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr2:83883827..83883951hg38UCSC Ensembl
chr2:84110951..84111075hg19UCSC Ensembl
Cytoband2p11.2
Allele length
AssemblyAllele length
hg38125
hg19125
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv14293195
SamplesNA19239
Known Genes
MethodSequencing
AnalysisMultiple analysis algorthms
PlatformIllumina HiSeq
Comments
ReferenceChaisson_et_al_2019
Pubmed ID30992455
Accession Number(s)nsv3526903
Frequency
Sample Size9
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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