A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1009872



Internal ID19099091
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr2:99223668..99308080hg38UCSC Ensembl
Innerchr2:99840131..99924543hg19UCSC Ensembl
Innerchr2:99206563..99290975hg18UCSC Ensembl
Cytoband2q11.2
Allele length
AssemblyAllele length
hg3884413
hg1984413
hg1884413
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv4030n100
Supporting Variantsnssv3580084, nssv3580082, nssv3580083, nssv3729166
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)nsv1009872
Frequency
Sample Size11257
Observed Gain4
Observed Loss0
Observed Complex0
Frequencyn/a


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