A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv588870



Internal ID16376279
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr22:26100656..26109252hg38UCSC Ensembl
Innerchr22:26496622..26505218hg19UCSC Ensembl
Innerchr22:24826622..24835218hg18UCSC Ensembl
Cytoband22q12.1
Allele length
AssemblyAllele length
hg388597
hg198597
hg188597
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv954548, nssv954549
Samples
Known GenesMIR1302-1
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)nsv588870
Frequency
Sample Size17421
Observed Gain0
Observed Loss2
Observed Complex0
Frequencyn/a


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