A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv561873



Internal ID16349282
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr13:62077951..62083202hg38UCSC Ensembl
Innerchr13:62652084..62657335hg19UCSC Ensembl
Innerchr13:61550085..61555336hg18UCSC Ensembl
Cytoband13q21.31
Allele length
AssemblyAllele length
hg385252
hg195252
hg185252
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv812344, nssv812346, nssv812345, nssv812343
Samples
Known Genes
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)nsv561873
Frequency
Sample Size17421
Observed Gain0
Observed Loss4
Observed Complex0
Frequencyn/a


Hosted by The Centre for Applied Genomics
Grant support for DGV
Please read the usage disclaimer