A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv3481731



Internal ID18723168
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr1:12806942..12858224hg38UCSC Ensembl
Innerchr1:12867078..12918079hg19UCSC Ensembl
Innerchr1:12789665..12840666hg18UCSC Ensembl
Cytoband1p36.21
Allele length
AssemblyAllele length
hg3851283
hg1951002
hg1851002
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv1010920
Supporting Variants
Samples
Known GenesHNRNPCL1, LOC649330, PRAMEF11, PRAMEF2
MethodSNP array
AnalysisAffymetrix SNP array copy number analysis
PlatformAffymetrix SNP Array 6.0
Comments
ReferenceCoe_et_al_2014
Pubmed ID25217958
Accession Number(s)nssv3481731
Frequency
Sample Size29084
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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