A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv951841



Internal ID16954028
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Outerchr10:104311343..104316942hg38UCSC Ensembl
Outerchr10:106071101..106076700hg19UCSC Ensembl
Cytoband10q25.1
Allele length
AssemblyAllele length
hg385600
hg195600
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv2998042
SamplesBILGI_BIOE
Known GenesITPRIP
MethodSequencing
Analysis
PlatformIllumina HiSeq 2000
Comments
ReferenceDogan_et_al_2014
Pubmed ID24416366
Accession Number(s)nsv951841
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