A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1055067



Internal ID18797598
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr14:100951479..100992723hg38UCSC Ensembl
Innerchr14:101417816..101459060hg19UCSC Ensembl
Innerchr14:100487569..100528813hg18UCSC Ensembl
Cytoband14q32.31
Allele length
AssemblyAllele length
hg3841245
hg1941245
hg1841245
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv3533549
Samples
Known GenesSNORD114-10, 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, SNORD114-30, 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)nsv1055067
Frequency
Sample Size29084
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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