A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv3210939



Internal ID22358664
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr15:78928299..78941537hg38UCSC Ensembl
chr15:79220641..79233879hg19UCSC Ensembl
Cytoband15q25.1
Allele length
AssemblyAllele length
hg3813239
hg1913239
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv14380317
SamplesHG00732
Known GenesCTSH
MethodSequencing
AnalysisMultiple analysis algorthms
PlatformIllumina HiSeq
Comments
ReferenceChaisson_et_al_2019
Pubmed ID30992455
Accession Number(s)nsv3210939
Frequency
Sample Size9
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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