A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv955197



Internal ID17304070
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Outerchr22:49991972..50017471hg38UCSC Ensembl
Outerchr22:50430401..50455900hg19UCSC Ensembl
Cytoband22q13.33
Allele length
AssemblyAllele length
hg3825500
hg1925500
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv3000843
SamplesBILGI_BIOE
Known GenesIL17REL
MethodSequencing
Analysis
PlatformIllumina HiSeq 2000
Comments
ReferenceDogan_et_al_2014
Pubmed ID24416366
Accession Number(s)nsv955197
Frequency
Sample Size1
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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