A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv951479



Internal ID17300353
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Outerchr9:67869055..67912254hg38UCSC Ensembl
Outerchr9:67936501..67979700hg19UCSC Ensembl
Cytoband9q13
Allele length
AssemblyAllele length
hg3843200
hg1943200
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv2996858
SamplesBILGI_BIOE
Known GenesANKRD20A1, ANKRD20A3
MethodSequencing
Analysis
PlatformIllumina HiSeq 2000
Comments
ReferenceDogan_et_al_2014
Pubmed ID24416366
Accession Number(s)nsv951479
Frequency
Sample Size1
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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