A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1044957



Internal ID19134176
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr11:54554865..54579484hg38UCSC Ensembl
Innerchr11:51539796..51564415hg19UCSC Ensembl
Innerchr11:51396372..51420991hg18UCSC Ensembl
Cytoband11p11.11
Allele length
AssemblyAllele length
hg3824620
hg1924620
hg1824620
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv1158n100
Supporting Variantsnssv3516814, nssv3504850
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)nsv1044957
Frequency
Sample Size11257
Observed Gain2
Observed Loss0
Observed Complex0
Frequencyn/a


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