A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv2999478



Internal ID16945744
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Outerchr9:67697582..67730356hg38UCSC Ensembl
Outerchr9:46363101..46394700hg19UCSC Ensembl
Cytoband9p11.2
Allele length
AssemblyAllele length
hg3832775
hg1931600
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv951169
Supporting Variants
SamplesBILGI_BIOE
Known GenesFAM27E1
MethodSequencing
Analysis
PlatformIllumina HiSeq 2000
Comments
ReferenceDogan_et_al_2014
Pubmed ID24416366
Accession Number(s)nssv2999478
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