A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv3202013



Internal ID22351235
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr7:107847479..107847536hg38UCSC Ensembl
chr7:107487924..107487981hg19UCSC Ensembl
Cytoband7q31.1
Allele length
AssemblyAllele length
hg3858
hg1958
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv14337530, nssv14337531, nssv14337532, nssv14337529
SamplesHG00731, HG00732, HG00513, HG00514
Known Genes
MethodSequencing
AnalysisMultiple analysis algorthms
PlatformIllumina HiSeq
Comments
ReferenceChaisson_et_al_2019
Pubmed ID30992455
Accession Number(s)nsv3202013
Frequency
Sample Size9
Observed Gain0
Observed Loss4
Observed Complex0
Frequencyn/a


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