A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv3000814



Internal ID17293766
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Outerchr22:43397295..43411794hg38UCSC Ensembl
Outerchr22:43793301..43807800hg19UCSC Ensembl
Cytoband22q13.2
Allele length
AssemblyAllele length
hg3814500
hg1914500
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv955168
Supporting Variants
SamplesBILGI_BIOE
Known Genes
MethodSequencing
Analysis
PlatformIllumina HiSeq 2000
Comments
ReferenceDogan_et_al_2014
Pubmed ID24416366
Accession Number(s)nssv3000814
Frequency
Sample Size1
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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