A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv951799



Internal ID16953986
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Outerchr9:133473579..133617678hg38UCSC Ensembl
Outerchr9:136338701..136482800hg19UCSC Ensembl
Cytoband9q34.2
Allele length
AssemblyAllele length
hg38144100
hg19144100
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv2997011
SamplesBILGI_BIOE
Known GenesADAMTSL2, FAM163B, SLC2A6, TMEM8C
MethodSequencing
Analysis
PlatformIllumina HiSeq 2000
Comments
ReferenceDogan_et_al_2014
Pubmed ID24416366
Accession Number(s)nsv951799
Frequency
Sample Size1
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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