A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv952705



Internal ID16954892
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Outerchr10:133211797..133290296hg38UCSC Ensembl
Outerchr10:135025301..135103800hg19UCSC Ensembl
Cytoband10q26.3
Allele length
AssemblyAllele length
hg3878500
hg1978500
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv2998094
SamplesBILGI_BIOE
Known GenesADAM8, KNDC1, MIR202, MIR202HG, TUBGCP2, UTF1, VENTX
MethodSequencing
Analysis
PlatformIllumina HiSeq 2000
Comments
ReferenceDogan_et_al_2014
Pubmed ID24416366
Accession Number(s)nsv952705
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