A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv951574



Internal ID16953761
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Outerchr10:46615417..46620816hg38UCSC Ensembl
Outerchr10:46928801..46934200hg19UCSC Ensembl
Cytoband10q11.22
Allele length
AssemblyAllele length
hg385400
hg195400
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv2997965
SamplesBILGI_BIOE
Known GenesFAM35BP
MethodSequencing
Analysis
PlatformIllumina HiSeq 2000
Comments
ReferenceDogan_et_al_2014
Pubmed ID24416366
Accession Number(s)nsv951574
Frequency
Sample Size1
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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