A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1023808



Internal ID19113025
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr6:27688270..27706575hg38UCSC Ensembl
Innerchr6:27656049..27674354hg19UCSC Ensembl
Innerchr6:27764028..27782333hg18UCSC Ensembl
Cytoband6p22.1
Allele length
AssemblyAllele length
hg3818306
hg1918306
hg1818306
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv3655762
Samples
Known GenesLINC01012
MethodSNP array
AnalysisAffymetrix SNP array copy number analysis
PlatformAffymetrix SNP Array 6.0
Comments
ReferenceCoe_et_al_2014
Pubmed ID25217958
Accession Number(s)nsv1023808
Frequency
Sample Size11257
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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