A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1045742



Internal ID19134961
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr11:55006405..55164277hg38UCSC Ensembl
Innerchr11:54773881..54931753hg19UCSC Ensembl
Innerchr11:54530457..54688329hg18UCSC Ensembl
Cytoband11q11
Allele length
AssemblyAllele length
hg38157873
hg19157873
hg18157873
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv1159n100
Supporting Variantsnssv3515518
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)nsv1045742
Frequency
Sample Size11257
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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