A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv3530135



Internal ID18828416
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr14:39893187..39964218hg38UCSC Ensembl
Innerchr14:40362391..40433422hg19UCSC Ensembl
Innerchr14:39432142..39503173hg18UCSC Ensembl
Cytoband14q21.1
Allele length
AssemblyAllele length
hg3871032
hg1971032
hg1871032
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv1035957
Supporting Variants
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)nssv3530135
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