A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv564875



Internal ID16352284
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr14:56713996..56729537hg38UCSC Ensembl
Innerchr14:57180714..57196255hg19UCSC Ensembl
Innerchr14:56250467..56266008hg18UCSC Ensembl
Cytoband14q22.3
Allele length
AssemblyAllele length
hg3815542
hg1915542
hg1815542
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv1149490
SamplesHGDP00158
Known Genes
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)nsv564875
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