A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv3194855



Internal ID22345117
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr7:32566018..32566334hg38UCSC Ensembl
chr7:32605630..32605946hg19UCSC Ensembl
Cytoband7p14.3
Allele length
AssemblyAllele length
hg38317
hg19317
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv14334650, nssv14334649
SamplesHG00512, HG00514
Known GenesAVL9
MethodSequencing
AnalysisMultiple analysis algorthms
PlatformIllumina HiSeq
Comments
ReferenceChaisson_et_al_2019
Pubmed ID30992455
Accession Number(s)nsv3194855
Frequency
Sample Size9
Observed Gain0
Observed Loss2
Observed Complex0
Frequencyn/a


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