A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv3221949



Internal ID22366171
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr11:7980367..7980814hg38UCSC Ensembl
chr11:8001914..8002361hg19UCSC Ensembl
Cytoband11p15.4
Allele length
AssemblyAllele length
hg38448
hg19448
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv14358141, nssv14358142
SamplesHG00512, NA19239
Known Genes
MethodSequencing
AnalysisMultiple analysis algorthms
PlatformIllumina HiSeq
Comments
ReferenceChaisson_et_al_2019
Pubmed ID30992455
Accession Number(s)nsv3221949
Frequency
Sample Size9
Observed Gain0
Observed Loss2
Observed Complex0
Frequencyn/a


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