A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv3582059



Internal ID18880340
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr2:77164013..77214142hg38UCSC Ensembl
Innerchr2:77391139..77441268hg19UCSC Ensembl
Innerchr2:77244647..77294776hg18UCSC Ensembl
Cytoband2p12
Allele length
AssemblyAllele length
hg3850130
hg1950130
hg1850130
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv1005392
Supporting Variants
Samples
Known GenesLRRTM4
MethodSNP array
AnalysisAffymetrix SNP array copy number analysis
PlatformAffymetrix SNP Array 6.0
Comments
ReferenceCoe_et_al_2014
Pubmed ID25217958
Accession Number(s)nssv3582059
Frequency
Sample Size11257
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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