A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv3208665



Internal ID22356865
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr1:15063769..15063824hg38UCSC Ensembl
chr1:15390265..15390320hg19UCSC Ensembl
Cytoband1p36.21
Allele length
AssemblyAllele length
hg3856
hg1956
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv14340119
SamplesNA19238
Known GenesKAZN
MethodSequencing
AnalysisMultiple analysis algorthms
PlatformIllumina HiSeq
Comments
ReferenceChaisson_et_al_2019
Pubmed ID30992455
Accession Number(s)nsv3208665
Frequency
Sample Size9
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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