A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv3466311



Internal ID18714996
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr1:12797714..12832443hg38UCSC Ensembl
Innerchr1:12857863..12892297hg19UCSC Ensembl
Innerchr1:12780450..12814884hg18UCSC Ensembl
Cytoband1p36.21
Allele length
AssemblyAllele length
hg3834730
hg1934435
hg1834435
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv1003521
Supporting Variants
Samples
Known GenesPRAMEF11
MethodSNP array
AnalysisAffymetrix SNP array copy number analysis
PlatformAffymetrix SNP Array 6.0
Comments
ReferenceCoe_et_al_2014
Pubmed ID25217958
Accession Number(s)nssv3466311
Frequency
Sample Size29084
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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