A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv3580866



Internal ID18532461
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr2:131314898..131521740hg38UCSC Ensembl
Innerchr2:132072471..132279313hg19UCSC Ensembl
Innerchr2:131788941..131995783hg18UCSC Ensembl
Cytoband2q21.1
Allele length
AssemblyAllele length
hg38206843
hg19206843
hg18206843
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv1011172
Supporting Variants
Samples
Known GenesLINC01120, LOC150776, LOC401010, MIR4784, MZT2A, RNU6-81P, TUBA3D, WTH3DI
MethodSNP array
AnalysisAffymetrix SNP array copy number analysis
PlatformAffymetrix SNP Array 6.0
Comments
ReferenceCoe_et_al_2014
Pubmed ID25217958
Accession Number(s)nssv3580866
Frequency
Sample Size29084
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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