A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv3525087



Internal ID22394463
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr2:25417533..25417763hg38UCSC Ensembl
chr2:25640402..25640632hg19UCSC Ensembl
Cytoband2p23.3
Allele length
AssemblyAllele length
hg38231
hg19231
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv14288935
SamplesHG00731
Known GenesDTNB
MethodSequencing
AnalysisMultiple analysis algorthms
PlatformIllumina HiSeq
Comments
ReferenceChaisson_et_al_2019
Pubmed ID30992455
Accession Number(s)nsv3525087
Frequency
Sample Size9
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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