A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv951231



Internal ID17300105
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Outerchr10:1037361..1046360hg38UCSC Ensembl
Outerchr10:1083301..1092300hg19UCSC Ensembl
Cytoband10p15.3
Allele length
AssemblyAllele length
hg389000
hg199000
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv2997067
SamplesBILGI_BIOE
Known GenesIDI1, IDI2-AS1
MethodSequencing
Analysis
PlatformIllumina HiSeq 2000
Comments
ReferenceDogan_et_al_2014
Pubmed ID24416366
Accession Number(s)nsv951231
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