A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv3516522



Internal ID18468117
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr11:75161747..75184196hg38UCSC Ensembl
Innerchr11:74872792..74895241hg19UCSC Ensembl
Innerchr11:74550440..74572889hg18UCSC Ensembl
Cytoband11q13.4
Allele length
AssemblyAllele length
hg3822450
hg1922450
hg1822450
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv1054122
Supporting Variants
Samples
Known GenesSLCO2B1
MethodSNP array
AnalysisAffymetrix SNP array copy number analysis
PlatformAffymetrix SNP Array 6.0
Comments
ReferenceCoe_et_al_2014
Pubmed ID25217958
Accession Number(s)nssv3516522
Frequency
Sample Size29084
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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