A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1045201



Internal ID19134420
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr14:86840375..86880778hg38UCSC Ensembl
Innerchr14:87306719..87347122hg19UCSC Ensembl
Innerchr14:86376472..86416875hg18UCSC Ensembl
Cytoband14q31.3
Allele length
AssemblyAllele length
hg3840404
hg1940404
hg1840404
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv3532552
Samples
Known Genes
MethodSNP array
AnalysisAffymetrix SNP array copy number analysis
PlatformAffymetrix SNP Array 6.0
Comments
ReferenceCoe_et_al_2014
Pubmed ID25217958
Accession Number(s)nsv1045201
Frequency
Sample Size11257
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


Hosted by The Centre for Applied Genomics
Grant support for DGV
Please read the usage disclaimer