A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv955199



Internal ID16957386
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Outerchr22:50149372..50320271hg38UCSC Ensembl
Outerchr22:50587801..50758700hg19UCSC Ensembl
Cytoband22q13.33
Allele length
AssemblyAllele length
hg38170900
hg19170900
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv3000845
SamplesBILGI_BIOE
Known GenesDENND6B, HDAC10, MAPK11, MAPK12, MOV10L1, PANX2, PLXNB2, SELO, TRABD, TUBGCP6
MethodSequencing
Analysis
PlatformIllumina HiSeq 2000
Comments
ReferenceDogan_et_al_2014
Pubmed ID24416366
Accession Number(s)nsv955199
Frequency
Sample Size1
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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