A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv3579480



Internal ID18877761
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr2:91460974..91737435hg38UCSC Ensembl
Innerchr2:91653350..91925461hg19UCSC Ensembl
Innerchr2:91017077..91289188hg18UCSC Ensembl
Cytoband2p11.1
Allele length
AssemblyAllele length
hg38276462
hg19272112
hg18272112
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv1003648
Supporting Variants
Samples
Known GenesLOC654342
MethodSNP array
AnalysisAffymetrix SNP array copy number analysis
PlatformAffymetrix SNP Array 6.0
Comments
ReferenceCoe_et_al_2014
Pubmed ID25217958
Accession Number(s)nssv3579480
Frequency
Sample Size11257
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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