A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1035826



Internal ID19125045
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr14:85383797..85432388hg38UCSC Ensembl
Innerchr14:85850141..85898732hg19UCSC Ensembl
Innerchr14:84919894..84968485hg18UCSC Ensembl
Cytoband14q31.3
Allele length
AssemblyAllele length
hg3848592
hg1948592
hg1848592
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv1949n100
Supporting Variantsnssv3713539
Samples
Known GenesLINC00911
MethodSNP array
AnalysisAffymetrix SNP array copy number analysis
PlatformAffymetrix SNP Array 6.0
Comments
ReferenceCoe_et_al_2014
Pubmed ID25217958
Accession Number(s)nsv1035826
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