A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1155106



Internal ID22085611
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr1:248585893..248633912hg38UCSC Ensembl
Outerchr1:248574146..248645256hg38UCSC Ensembl
Innerchr1:248749194..248797213hg19UCSC Ensembl
Outerchr1:248737447..248808557hg19UCSC Ensembl
Cytoband1q44
Allele length
AssemblyAllele length
hg3871111
hg1971111
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv27n97
Supporting Variantsnssv4007534, nssv4007552, nssv4007548, nssv4007550, nssv4007542, nssv4007529, nssv4007541, nssv4007551, nssv4007559, nssv4007533, nssv4007544, nssv4007558, nssv4007531, nssv4007556, nssv4007540, nssv4007545, nssv4007532, nssv4007557, nssv4007555, nssv4007528, nssv4007536, nssv4007530, nssv4007535, nssv4007549, nssv4007554, nssv4007560, nssv4007538, nssv4007553, nssv4007539, nssv4007547, nssv4007546, nssv4007537, nssv4007543
Samples
Known GenesOR2T10, OR2T11, OR2T34, OR2T35
MethodSNP array
AnalysisDefault settings
Platform
Comments
ReferenceLou_et_al_2014
Pubmed ID25026903
Accession Number(s)nsv1155106
Frequency
Sample Size131
Observed Gain0
Observed Loss33
Observed Complex0
Frequencyn/a


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