A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv565877



Internal ID16353286
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr14:101458153..101459234hg38UCSC Ensembl
Innerchr14:101924490..101925571hg19UCSC Ensembl
Innerchr14:100994243..100995324hg18UCSC Ensembl
Cytoband14q32.31
Allele length
AssemblyAllele length
hg381082
hg191082
hg181082
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv3920n54
Supporting Variantsnssv833712
Samples
Known Genes
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)nsv565877
Frequency
Sample Size17421
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


Hosted by The Centre for Applied Genomics
Grant support for DGV
Please read the usage disclaimer