A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv950881



Internal ID17299755
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Outerchr9:88848886..88855485hg38UCSC Ensembl
Outerchr9:91463801..91470400hg19UCSC Ensembl
Cytoband9q22.1
Allele length
AssemblyAllele length
hg386600
hg196600
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv2996915
SamplesBILGI_BIOE
Known Genes
MethodSequencing
Analysis
PlatformIllumina HiSeq 2000
Comments
ReferenceDogan_et_al_2014
Pubmed ID24416366
Accession Number(s)nsv950881
Frequency
Sample Size1
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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