A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv564753



Internal ID16352162
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr14:46400594..46537686hg38UCSC Ensembl
Innerchr14:46869797..47006889hg19UCSC Ensembl
Innerchr14:45939547..46076639hg18UCSC Ensembl
Cytoband14q21.2
Allele length
AssemblyAllele length
hg38137093
hg19137093
hg18137093
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv827690
Samples
Known GenesLINC00871
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)nsv564753
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