A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1036978



Internal ID19126197
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr11:99722065..99752416hg38UCSC Ensembl
Innerchr11:99592796..99623147hg19UCSC Ensembl
Innerchr11:99098006..99128357hg18UCSC Ensembl
Cytoband11q22.1
Allele length
AssemblyAllele length
hg3830352
hg1930352
hg1830352
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv3710735
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)nsv1036978
Frequency
Sample Size11257
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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