A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv3222573



Internal ID22366609
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr15:96454382..96461054hg38UCSC Ensembl
chr15:96997612..97004284hg19UCSC Ensembl
Cytoband15q26.2
Allele length
AssemblyAllele length
hg386673
hg196673
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv14390962, nssv14374080
SamplesHG00513, HG00514
Known Genes
MethodSequencing
AnalysisMultiple analysis algorthms
PlatformIllumina HiSeq
Comments
ReferenceChaisson_et_al_2019
Pubmed ID30992455
Accession Number(s)nsv3222573
Frequency
Sample Size9
Observed Gain0
Observed Loss2
Observed Complex0
Frequencyn/a


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