A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv955195



Internal ID17304068
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Outerchr22:49926653..49952952hg38UCSC Ensembl
Outerchr22:50320301..50346600hg19UCSC Ensembl
Cytoband22q13.33
Allele length
AssemblyAllele length
hg3826300
hg1926300
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv3000841
SamplesBILGI_BIOE
Known GenesCRELD2
MethodSequencing
Analysis
PlatformIllumina HiSeq 2000
Comments
ReferenceDogan_et_al_2014
Pubmed ID24416366
Accession Number(s)nsv955195
Frequency
Sample Size1
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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