A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv549610



Internal ID16337019
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr1:247991310..247991997hg38UCSC Ensembl
Innerchr1:248154612..248155299hg19UCSC Ensembl
Innerchr1:246221235..246221922hg18UCSC Ensembl
Cytoband1q44
Allele length
AssemblyAllele length
hg38688
hg19688
hg18688
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv901n54
Supporting Variantsnssv739699, nssv739702, nssv739694, nssv739701, nssv739695, nssv739691, nssv739704, nssv739700, nssv739698, nssv739703, nssv739693, nssv739692, nssv739696, nssv739697
Samples
Known GenesOR2L13
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)nsv549610
Frequency
Sample Size17421
Observed Gain0
Observed Loss14
Observed Complex0
Frequencyn/a


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