A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1035178



Internal ID19124397
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr14:22151963..22484618hg38UCSC Ensembl
Innerchr14:22619918..22953607hg19UCSC Ensembl
Innerchr14:21689758..22023447hg18UCSC Ensembl
Cytoband14q11.2
Allele length
AssemblyAllele length
hg38332656
hg19333690
hg18333690
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv1805n100
Supporting Variantsnssv3532204
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)nsv1035178
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