A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv561384



Internal ID16348793
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr13:26732521..26733865hg38UCSC Ensembl
Innerchr13:27306658..27308002hg19UCSC Ensembl
Innerchr13:26204658..26206002hg18UCSC Ensembl
Cytoband13q12.13
Allele length
AssemblyAllele length
hg381345
hg191345
hg181345
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv3099n54
Supporting Variantsnssv807236
Samples
Known Genes
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)nsv561384
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