A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1035568



Internal ID18778099
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr14:100939598..100992723hg38UCSC Ensembl
Innerchr14:101405935..101459060hg19UCSC Ensembl
Innerchr14:100475688..100528813hg18UCSC Ensembl
Cytoband14q32.31
Allele length
AssemblyAllele length
hg3853126
hg1953126
hg1853126
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv1976n100
Supporting Variantsnssv3533540, nssv3533542, nssv3533543, nssv3533541
Samples
Known GenesSNORD113-6, 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, SNORD114-30, 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)nsv1035568
Frequency
Sample Size29084
Observed Gain0
Observed Loss4
Observed Complex0
Frequencyn/a


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