A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1000522



Internal ID18743053
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr1:247664654..248032454hg38UCSC Ensembl
Innerchr1:247827956..248195756hg19UCSC Ensembl
Innerchr1:245894579..246262379hg18UCSC Ensembl
Cytoband1q44
Allele length
AssemblyAllele length
hg38367801
hg19367801
hg18367801
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv605n100
Supporting Variantsnssv3500592
Samples
Known GenesOR11L1, OR13G1, OR14A16, OR1C1, OR2AK2, OR2L13, OR2L1P, OR2L5, OR2L8, OR2T8, OR2W3, OR6F1, TRIM58
MethodSNP array
AnalysisAffymetrix SNP array copy number analysis
PlatformAffymetrix SNP Array 6.0
Comments
ReferenceCoe_et_al_2014
Pubmed ID25217958
Accession Number(s)nsv1000522
Frequency
Sample Size29084
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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