A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv569578



Internal ID16356987
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr15:57202862..57267189hg38UCSC Ensembl
Innerchr15:57495060..57559387hg19UCSC Ensembl
Innerchr15:55282352..55346679hg18UCSC Ensembl
Cytoband15q21.3
Allele length
AssemblyAllele length
hg3864328
hg1964328
hg1864328
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv1149222
Samples1780854023_A
Known GenesTCF12
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)nsv569578
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