A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv950938



Internal ID16953125
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Outerchr9:121336023..121366322hg38UCSC Ensembl
Outerchr9:124098301..124128600hg19UCSC Ensembl
Cytoband9q33.2
Allele length
AssemblyAllele length
hg3830300
hg1930300
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv2996967
SamplesBILGI_BIOE
Known GenesSTOM
MethodSequencing
Analysis
PlatformIllumina HiSeq 2000
Comments
ReferenceDogan_et_al_2014
Pubmed ID24416366
Accession Number(s)nsv950938
Frequency
Sample Size1
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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