A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1038895



Internal ID18781426
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr14:20880785..20941810hg38UCSC Ensembl
Innerchr14:21348944..21409969hg19UCSC Ensembl
Innerchr14:20418784..20479809hg18UCSC Ensembl
Cytoband14q11.2
Allele length
AssemblyAllele length
hg3861026
hg1961026
hg1861026
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv1799n100
Supporting Variantsnssv3530751
Samples
Known GenesECRP, RNASE3
MethodSNP array
AnalysisAffymetrix SNP array copy number analysis
PlatformAffymetrix SNP Array 6.0
Comments
ReferenceCoe_et_al_2014
Pubmed ID25217958
Accession Number(s)nsv1038895
Frequency
Sample Size29084
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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