A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv604501



Internal ID16045224
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr6:110248622..110249782hg38UCSC Ensembl
Innerchr6:110569825..110570985hg19UCSC Ensembl
Innerchr6:110676518..110677678hg18UCSC Ensembl
Cytoband6q21
Allele length
AssemblyAllele length
hg381161
hg191161
hg181161
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv10908n54
Supporting Variantsnssv1072007
Samples
Known GenesMETTL24
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)nsv604501
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