A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv955502



Internal ID17304375
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Outerchr22:38923650..38923812hg38UCSC Ensembl
Outerchr22:39319655..39319817hg19UCSC Ensembl
Cytoband22q13.1
Allele length
AssemblyAllele length
hg38163
hg19163
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv3004417
SamplesBILGI_BIOE
Known Genes
MethodSequencing
Analysis
PlatformIllumina HiSeq 2000
Comments
ReferenceDogan_et_al_2014
Pubmed ID24416366
Accession Number(s)nsv955502
Frequency
Sample Size1
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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