A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv950914



Internal ID16953101
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Outerchr9:97850419..97857618hg38UCSC Ensembl
Outerchr9:100612701..100619900hg19UCSC Ensembl
Cytoband9q22.33
Allele length
AssemblyAllele length
hg387200
hg197200
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv2996945
SamplesBILGI_BIOE
Known GenesFOXE1
MethodSequencing
Analysis
PlatformIllumina HiSeq 2000
Comments
ReferenceDogan_et_al_2014
Pubmed ID24416366
Accession Number(s)nsv950914
Frequency
Sample Size1
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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