A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv951169



Internal ID16953356
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 StatusM
Merged Variants
Supporting Variantsnssv2999478
SamplesBILGI_BIOE
Known GenesFAM27E1
MethodSequencing
Analysis
PlatformIllumina HiSeq 2000
Comments
ReferenceDogan_et_al_2014
Pubmed ID24416366
Accession Number(s)nsv951169
Frequency
Sample Size1
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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