A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv951790



Internal ID17300664
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Outerchr9:131256914..131262513hg38UCSC Ensembl
Outerchr9:134132301..134137900hg19UCSC Ensembl
Cytoband9q34.13
Allele length
AssemblyAllele length
hg385600
hg195600
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv2997002
SamplesBILGI_BIOE
Known GenesFAM78A
MethodSequencing
Analysis
PlatformIllumina HiSeq 2000
Comments
ReferenceDogan_et_al_2014
Pubmed ID24416366
Accession Number(s)nsv951790
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