A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1037186



Internal ID19126405
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr11:99161361..99218359hg38UCSC Ensembl
Innerchr11:99032092..99089090hg19UCSC Ensembl
Innerchr11:98537302..98594300hg18UCSC Ensembl
Cytoband11q22.1
Allele length
AssemblyAllele length
hg3856999
hg1956999
hg1856999
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv1263n100
Supporting Variantsnssv3504782
Samples
Known GenesCNTN5
MethodSNP array
AnalysisAffymetrix SNP array copy number analysis
PlatformAffymetrix SNP Array 6.0
Comments
ReferenceCoe_et_al_2014
Pubmed ID25217958
Accession Number(s)nsv1037186
Frequency
Sample Size11257
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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