A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv950894



Internal ID17299768
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Outerchr9:92745719..92749018hg38UCSC Ensembl
Outerchr9:95508001..95511300hg19UCSC Ensembl
Cytoband9q22.31
Allele length
AssemblyAllele length
hg383300
hg193300
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv2996927
SamplesBILGI_BIOE
Known GenesBICD2
MethodSequencing
Analysis
PlatformIllumina HiSeq 2000
Comments
ReferenceDogan_et_al_2014
Pubmed ID24416366
Accession Number(s)nsv950894
Frequency
Sample Size1
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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