A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv954560



Internal ID15901830
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr22:30440326..30472431hg38UCSC Ensembl
Innerchr22:30836313..30868418hg19UCSC Ensembl
Innerchr22:29166313..29198418hg18UCSC Ensembl
Cytoband22q12.2
Allele length
AssemblyAllele length
hg3832106
hg1932106
hg1832106
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv588886
Supporting Variants
Samples
Known GenesSEC14L3
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)nssv954560
Frequency
Sample Size17421
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


Hosted by The Centre for Applied Genomics
Grant support for DGV
Please read the usage disclaimer