A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv3528564



Internal ID22397952
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr17:7852396..7852448hg38UCSC Ensembl
chr17:7755714..7755766hg19UCSC Ensembl
Cytoband17p13.1
Allele length
AssemblyAllele length
hg3853
hg1953
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv14381032, nssv14377277
SamplesHG00731, HG00733
Known GenesKDM6B
MethodSequencing
AnalysisMultiple analysis algorthms
PlatformIllumina HiSeq
Comments
ReferenceChaisson_et_al_2019
Pubmed ID30992455
Accession Number(s)nsv3528564
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