A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1053355



Internal ID19142574
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr14:40737298..41068990hg38UCSC Ensembl
Innerchr14:41206503..41538195hg19UCSC Ensembl
Innerchr14:40276253..40607945hg18UCSC Ensembl
Cytoband14q21.1
Allele length
AssemblyAllele length
hg38331693
hg19331693
hg18331693
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv1880n100
Supporting Variantsnssv3530154
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)nsv1053355
Frequency
Sample Size11257
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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