A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv565027



Internal ID16352436
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr14:70221529..70222673hg38UCSC Ensembl
Innerchr14:70688246..70689390hg19UCSC Ensembl
Innerchr14:69757999..69759143hg18UCSC Ensembl
Cytoband14q24.2
Allele length
AssemblyAllele length
hg381145
hg191145
hg181145
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv3748n54
Supporting Variantsnssv829009, nssv828994, nssv828986, nssv829024, nssv828998, nssv829011, nssv829023, nssv828995, nssv829004, nssv829025, nssv829013, nssv828992, nssv828997, nssv828999, nssv829001, nssv828989, nssv829014, nssv829006, nssv829003, nssv828988, nssv829008, nssv829019, nssv828993, nssv829012, nssv829007, nssv828990, nssv829018, nssv829016, nssv829022, nssv829002, nssv829010, nssv829000, nssv829021, nssv829027, nssv829028, nssv828991, nssv829005, nssv828996, nssv828987, nssv829020, nssv829017, nssv829026, nssv829015
Samples
Known Genes
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)nsv565027
Frequency
Sample Size17421
Observed Gain0
Observed Loss43
Observed Complex0
Frequencyn/a


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