A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv3580090



Internal ID18878371
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr2:99231427..99308080hg38UCSC Ensembl
Innerchr2:99847890..99924543hg19UCSC Ensembl
Innerchr2:99214322..99290975hg18UCSC Ensembl
Cytoband2q11.2
Allele length
AssemblyAllele length
hg3876654
hg1976654
hg1876654
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv1007566
Supporting Variants
Samples
Known GenesLYG1, LYG2
MethodSNP array
AnalysisAffymetrix SNP array copy number analysis
PlatformAffymetrix SNP Array 6.0
Comments
ReferenceCoe_et_al_2014
Pubmed ID25217958
Accession Number(s)nssv3580090
Frequency
Sample Size11257
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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