A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv557019



Internal ID15997742
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr12:2105687..2106885hg38UCSC Ensembl
Innerchr12:2214853..2216051hg19UCSC Ensembl
Innerchr12:2085114..2086312hg18UCSC Ensembl
Cytoband12p13.33
Allele length
AssemblyAllele length
hg381199
hg191199
hg181199
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv2281n54
Supporting Variantsnssv786422
Samples
Known GenesCACNA1C
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)nsv557019
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