A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv951699



Internal ID16953886
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Outerchr9:34553903..34574802hg38UCSC Ensembl
Outerchr9:34553901..34574800hg19UCSC Ensembl
Cytoband9p13.3
Allele length
AssemblyAllele length
hg3820900
hg1920900
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv2999388
SamplesBILGI_BIOE
Known GenesCNTFR, CNTFR-AS1
MethodSequencing
Analysis
PlatformIllumina HiSeq 2000
Comments
ReferenceDogan_et_al_2014
Pubmed ID24416366
Accession Number(s)nsv951699
Frequency
Sample Size1
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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