A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv3504782



Internal ID18803063
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 StatusS
Merged Variantsnsv1037186
Supporting Variants
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)nssv3504782
Frequency
Sample Size11257
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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