A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv516629



Internal ID15097236
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr11:133122804..133134954hg38UCSC Ensembl
Innerchr11:132992699..133004849hg19UCSC Ensembl
Innerchr11:132497909..132510059hg18UCSC Ensembl
Innerchr11:132497909..132510059hg17UCSC Ensembl
Cytoband11q25
Allele length
AssemblyAllele length
hg3812151
hg1912151
hg1812151
hg1712151
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv85n21
Supporting Variantsnssv688821, nssv686347, nssv669702, nssv678588, nssv662375, nssv674925, nssv655496, nssv684469, nssv675105, nssv695280
Samples
Known GenesOPCML
MethodSNP array
AnalysisSample-level CNVs
PlatformGPL6434
Comments
ReferenceShaikh_et_al_2009
Pubmed ID19592680
Accession Number(s)nsv516629
Frequency
Sample Size2026
Observed Gain0
Observed Loss10
Observed Complex0
Frequencyn/a


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