A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv956109



Internal ID16958296
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Outerchr9:112502394..112502458hg38UCSC Ensembl
Outerchr9:115264674..115264738hg19UCSC Ensembl
Cytoband9q32
Allele length
AssemblyAllele length
hg3865
hg1965
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv3002381
SamplesBILGI_BIOE
Known GenesKIAA1958
MethodSequencing
Analysis
PlatformIllumina HiSeq 2000
Comments
ReferenceDogan_et_al_2014
Pubmed ID24416366
Accession Number(s)nsv956109
Frequency
Sample Size1
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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