A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1041628



Internal ID19130847
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr11:55006405..55243656hg38UCSC Ensembl
Innerchr11:54773881..55011132hg19UCSC Ensembl
Innerchr11:54530457..54767708hg18UCSC Ensembl
Cytoband11q11
Allele length
AssemblyAllele length
hg38237252
hg19237252
hg18237252
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv1165n100
Supporting Variantsnssv3508321, nssv3510724, nssv3515161
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)nsv1041628
Frequency
Sample Size11257
Observed Gain3
Observed Loss0
Observed Complex0
Frequencyn/a


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