A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv952354



Internal ID16954541
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Outerchr17:63432740..63462739hg38UCSC Ensembl
Outerchr17:61510101..61540100hg19UCSC Ensembl
Cytoband17q23.3
Allele length
AssemblyAllele length
hg3830000
hg1930000
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv2998787
SamplesBILGI_BIOE
Known GenesCYB561
MethodSequencing
Analysis
PlatformIllumina HiSeq 2000
Comments
ReferenceDogan_et_al_2014
Pubmed ID24416366
Accession Number(s)nsv952354
Frequency
Sample Size1
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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