A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv955467



Internal ID17304340
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Outerchr22:35249138..35250109hg38UCSC Ensembl
Outerchr22:35645131..35646102hg19UCSC Ensembl
Cytoband22q12.3
Allele length
AssemblyAllele length
hg38972
hg19972
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv3003357
SamplesBILGI_BIOE
Known Genes
MethodSequencing
Analysis
PlatformIllumina HiSeq 2000
Comments
ReferenceDogan_et_al_2014
Pubmed ID24416366
Accession Number(s)nsv955467
Frequency
Sample Size1
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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