A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv950929



Internal ID16953116
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Outerchr9:113593221..113602120hg38UCSC Ensembl
Outerchr9:116355501..116364400hg19UCSC Ensembl
Cytoband9q32
Allele length
AssemblyAllele length
hg388900
hg198900
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv2996959
SamplesBILGI_BIOE
Known GenesRGS3
MethodSequencing
Analysis
PlatformIllumina HiSeq 2000
Comments
ReferenceDogan_et_al_2014
Pubmed ID24416366
Accession Number(s)nsv950929
Frequency
Sample Size1
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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