A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv557473



Internal ID15998196
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr12:10428209..10446385hg38UCSC Ensembl
Innerchr12:10580808..10598984hg19UCSC Ensembl
Innerchr12:10472075..10490251hg18UCSC Ensembl
Cytoband12p13.2
Allele length
AssemblyAllele length
hg3818177
hg1918177
hg1818177
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv2360n54
Supporting Variantsnssv788040, nssv788041, nssv788039
Samples
Known GenesKLRC1, KLRC2
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)nsv557473
Frequency
Sample Size17421
Observed Gain0
Observed Loss3
Observed Complex0
Frequencyn/a


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