A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv588994



Internal ID16376403
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr22:37352354..37353906hg38UCSC Ensembl
Innerchr22:37748394..37749946hg19UCSC Ensembl
Innerchr22:36078340..36079892hg18UCSC Ensembl
Cytoband22q13.1
Allele length
AssemblyAllele length
hg381553
hg191553
hg181553
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv8101n54
Supporting Variantsnssv956678, nssv956690, nssv956694, nssv956686, nssv956702, nssv956681, nssv956679, nssv956688, nssv956675, nssv956673, nssv956677, nssv956683, nssv956693, nssv956672, nssv956680, nssv956670, nssv956687, nssv956682, nssv956701, nssv956676, nssv956698, nssv956703, nssv956695, nssv956700, nssv956696, nssv956691, nssv956689, nssv956674, nssv956692, nssv956684, nssv956671, nssv956685, nssv956697, nssv956699
Samples
Known Genes
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)nsv588994
Frequency
Sample Size17421
Observed Gain0
Observed Loss34
Observed Complex0
Frequencyn/a


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