A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1041578



Internal ID19130797
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr11:55006405..55168113hg38UCSC Ensembl
Innerchr11:54773881..54935589hg19UCSC Ensembl
Innerchr11:54530457..54692165hg18UCSC Ensembl
Cytoband11q11
Allele length
AssemblyAllele length
hg38161709
hg19161709
hg18161709
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv1159n100
Supporting Variantsnssv3513219
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)nsv1041578
Frequency
Sample Size11257
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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