A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1048771



Internal ID19137990
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr14:22177786..22478293hg38UCSC Ensembl
Innerchr14:22645683..22947282hg19UCSC Ensembl
Innerchr14:21715523..22017122hg18UCSC Ensembl
Cytoband14q11.2
Allele length
AssemblyAllele length
hg38300508
hg19301600
hg18301600
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv1805n100
Supporting Variantsnssv3532241
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)nsv1048771
Frequency
Sample Size11257
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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