A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1054902



Internal ID19144121
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr14:40738095..41068990hg38UCSC Ensembl
Innerchr14:41207300..41538195hg19UCSC Ensembl
Innerchr14:40277050..40607945hg18UCSC Ensembl
Cytoband14q21.1
Allele length
AssemblyAllele length
hg38330896
hg19330896
hg18330896
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv1880n100
Supporting Variantsnssv3530155
Samples
Known GenesLOC644919
MethodSNP array
AnalysisAffymetrix SNP array copy number analysis
PlatformAffymetrix SNP Array 6.0
Comments
ReferenceCoe_et_al_2014
Pubmed ID25217958
Accession Number(s)nsv1054902
Frequency
Sample Size11257
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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