A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1051890



Internal ID19141109
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr14:20893865..20957189hg38UCSC Ensembl
Innerchr14:21362024..21425348hg19UCSC Ensembl
Innerchr14:20431864..20495188hg18UCSC Ensembl
Cytoband14q11.2
Allele length
AssemblyAllele length
hg3863325
hg1963325
hg1863325
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv1802n100
Supporting Variantsnssv3532113, nssv3532118, nssv3532111, nssv3532108, nssv3532106, nssv3532104, nssv3532102, nssv3532107, nssv3532112, nssv3532109, nssv3532117, nssv3532116, nssv3532105, nssv3532114, nssv3532115, nssv3532103, nssv3532110
Samples
Known GenesECRP, RNASE2
MethodSNP array
AnalysisAffymetrix SNP array copy number analysis
PlatformAffymetrix SNP Array 6.0
Comments
ReferenceCoe_et_al_2014
Pubmed ID25217958
Accession Number(s)nsv1051890
Frequency
Sample Size11257
Observed Gain0
Observed Loss17
Observed Complex0
Frequencyn/a


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