A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1053887



Internal ID18796418
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr14:100915376..100991447hg38UCSC Ensembl
Innerchr14:101381713..101457784hg19UCSC Ensembl
Innerchr14:100451466..100527537hg18UCSC Ensembl
Cytoband14q32.2
Allele length
AssemblyAllele length
hg3876072
hg1976072
hg1876072
Variant TypeCNV gain+loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv1973n100
Supporting Variantsnssv3533467, nssv3533468, nssv3533466, nssv3533465, nssv3533464, nssv3533461, nssv3533463, nssv3533462
Samples
Known GenesSNORD113-1, SNORD113-2, SNORD113-3, SNORD113-4, SNORD113-5, SNORD113-6, SNORD113-7, SNORD113-8, SNORD113-9, SNORD114-1, SNORD114-10, SNORD114-11, SNORD114-12, SNORD114-13, SNORD114-14, SNORD114-15, SNORD114-16, SNORD114-17, SNORD114-18, SNORD114-19, SNORD114-2, SNORD114-20, SNORD114-21, SNORD114-22, SNORD114-23, SNORD114-24, SNORD114-25, SNORD114-26, SNORD114-27, SNORD114-28, SNORD114-29, SNORD114-3, SNORD114-4, SNORD114-5, SNORD114-6, SNORD114-7, SNORD114-8, SNORD114-9
MethodSNP array
AnalysisAffymetrix SNP array copy number analysis
PlatformAffymetrix SNP Array 6.0
Comments
ReferenceCoe_et_al_2014
Pubmed ID25217958
Accession Number(s)nsv1053887
Frequency
Sample Size29084
Observed Gain1
Observed Loss7
Observed Complex0
Frequencyn/a


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