A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1048855



Internal ID19138074
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr14:42503822..42615283hg38UCSC Ensembl
Innerchr14:42973025..43084486hg19UCSC Ensembl
Innerchr14:42042775..42154236hg18UCSC Ensembl
Cytoband14q21.1
Allele length
AssemblyAllele length
hg38111462
hg19111462
hg18111462
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv3530212
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)nsv1048855
Frequency
Sample Size11257
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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