A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv3200347



Internal ID22349812
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr4:109693433..109694022hg38UCSC Ensembl
chr4:110614589..110615178hg19UCSC Ensembl
Cytoband4q25
Allele length
AssemblyAllele length
hg38590
hg19590
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv14314804
SamplesNA19240
Known GenesCASP6
MethodSequencing
AnalysisMultiple analysis algorthms
PlatformIllumina HiSeq
Comments
ReferenceChaisson_et_al_2019
Pubmed ID30992455
Accession Number(s)nsv3200347
Frequency
Sample Size9
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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