A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv562630



Internal ID16350039
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr13:87550822..87619348hg38UCSC Ensembl
Innerchr13:88203077..88271603hg19UCSC Ensembl
Innerchr13:87001078..87069604hg18UCSC Ensembl
Cytoband13q31.2
Allele length
AssemblyAllele length
hg3868527
hg1968527
hg1868527
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv816742, nssv816741
Samples
Known GenesMIR4500, MIR4500HG
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)nsv562630
Frequency
Sample Size17421
Observed Gain0
Observed Loss2
Observed Complex0
Frequencyn/a


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