A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv3528646



Internal ID18826927
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr14:38483785..38575109hg38UCSC Ensembl
Innerchr14:38952989..39044313hg19UCSC Ensembl
Innerchr14:38022740..38114064hg18UCSC Ensembl
Cytoband14q21.1
Allele length
AssemblyAllele length
hg3891325
hg1991325
hg1891325
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv1051499
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)nssv3528646
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