A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1048773



Internal ID19137992
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr14:39891162..39964218hg38UCSC Ensembl
Innerchr14:40360366..40433422hg19UCSC Ensembl
Innerchr14:39430117..39503173hg18UCSC Ensembl
Cytoband14q21.1
Allele length
AssemblyAllele length
hg3873057
hg1973057
hg1873057
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv1876n100
Supporting Variantsnssv3530134
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)nsv1048773
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