A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1045881



Internal ID19135100
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr11:107243089..107257288hg38UCSC Ensembl
Innerchr11:107113815..107128014hg19UCSC Ensembl
Innerchr11:106619025..106633224hg18UCSC Ensembl
Cytoband11q22.3
Allele length
AssemblyAllele length
hg3814200
hg1914200
hg1814200
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv3516002, nssv3509979, nssv3518976
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)nsv1045881
Frequency
Sample Size11257
Observed Gain0
Observed Loss3
Observed Complex0
Frequencyn/a


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