A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1053889



Internal ID19143108
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr14:22162256..22473159hg38UCSC Ensembl
Innerchr14:22630152..22942149hg19UCSC Ensembl
Innerchr14:21699992..22011989hg18UCSC Ensembl
Cytoband14q11.2
Allele length
AssemblyAllele length
hg38310904
hg19311998
hg18311998
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv1805n100
Supporting Variantsnssv3532223
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)nsv1053889
Frequency
Sample Size11257
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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