A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv564876



Internal ID16352285
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr14:56713996..56737237hg38UCSC Ensembl
Innerchr14:57180714..57203955hg19UCSC Ensembl
Innerchr14:56250467..56273708hg18UCSC Ensembl
Cytoband14q22.3
Allele length
AssemblyAllele length
hg3823242
hg1923242
hg1823242
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv828202
Samples
Known Genes
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)nsv564876
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