A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv3511738



Internal ID18810019
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr11:97107874..97175867hg38UCSC Ensembl
Innerchr11:96978874..97046867hg19UCSC Ensembl
Innerchr11:96484084..96552077hg18UCSC Ensembl
Cytoband11q21
Allele length
AssemblyAllele length
hg3867994
hg1967994
hg1867994
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv1040083
Supporting Variants
Samples
Known Genes
MethodSNP array
AnalysisAffymetrix SNP array copy number analysis
PlatformAffymetrix SNP Array 6.0
Comments
ReferenceCoe_et_al_2014
Pubmed ID25217958
Accession Number(s)nssv3511738
Frequency
Sample Size11257
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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