A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv562569



Internal ID16349978
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr13:85049548..85182275hg38UCSC Ensembl
Innerchr13:85623683..85756410hg19UCSC Ensembl
Innerchr13:84521684..84654411hg18UCSC Ensembl
Cytoband13q31.1
Allele length
AssemblyAllele length
hg38132728
hg19132728
hg18132728
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv1148552
SamplesNINDS_160
Known Genes
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)nsv562569
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