A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv3192216



Internal ID22342829
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr7:85314269..85316323hg38UCSC Ensembl
chr7:84943585..84945639hg19UCSC Ensembl
Cytoband7q21.11
Allele length
AssemblyAllele length
hg382055
hg192055
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv14335252, nssv14335251
SamplesHG00732, HG00733
Known Genes
MethodSequencing
AnalysisMultiple analysis algorthms
PlatformIllumina HiSeq
Comments
ReferenceChaisson_et_al_2019
Pubmed ID30992455
Accession Number(s)nsv3192216
Frequency
Sample Size9
Observed Gain0
Observed Loss2
Observed Complex0
Frequencyn/a


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