A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv3529497



Internal ID22398889
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr17:75095746..75096621hg38UCSC Ensembl
chr17:73091841..73092716hg19UCSC Ensembl
Cytoband17q25.1
Allele length
AssemblyAllele length
hg38876
hg19876
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv14281766, nssv14281767
SamplesNA19239, NA19240
Known GenesSLC16A5
MethodSequencing
AnalysisMultiple analysis algorthms
PlatformIllumina HiSeq
Comments
ReferenceChaisson_et_al_2019
Pubmed ID30992455
Accession Number(s)nsv3529497
Frequency
Sample Size9
Observed Gain0
Observed Loss2
Observed Complex0
Frequencyn/a


Hosted by The Centre for Applied Genomics
Grant support for DGV
Please read the usage disclaimer