A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1052123



Internal ID19141342
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr11:85714813..85760089hg38UCSC Ensembl
Innerchr11:85425856..85471132hg19UCSC Ensembl
Innerchr11:85103504..85148780hg18UCSC Ensembl
Cytoband11q14.1
Allele length
AssemblyAllele length
hg3845277
hg1945277
hg1845277
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv1245n100
Supporting Variantsnssv3521409, nssv3518408, nssv3521042
Samples
Known GenesSYTL2
MethodSNP array
AnalysisAffymetrix SNP array copy number analysis
PlatformAffymetrix SNP Array 6.0
Comments
ReferenceCoe_et_al_2014
Pubmed ID25217958
Accession Number(s)nsv1052123
Frequency
Sample Size11257
Observed Gain0
Observed Loss3
Observed Complex0
Frequencyn/a


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