A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv3516341



Internal ID18467936
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr11:67730549..67964706hg38UCSC Ensembl
Innerchr11:67498020..67732177hg19UCSC Ensembl
Innerchr11:67254596..67488753hg18UCSC Ensembl
Cytoband11q13.2
Allele length
AssemblyAllele length
hg38234158
hg19234158
hg18234158
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv1044670
Supporting Variants
Samples
Known GenesFAM86C2P
MethodSNP array
AnalysisAffymetrix SNP array copy number analysis
PlatformAffymetrix SNP Array 6.0
Comments
ReferenceCoe_et_al_2014
Pubmed ID25217958
Accession Number(s)nssv3516341
Frequency
Sample Size29084
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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