A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv604514



Internal ID16391923
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr6:110249472..110250312hg38UCSC Ensembl
Innerchr6:110570675..110571515hg19UCSC Ensembl
Innerchr6:110677368..110678208hg18UCSC Ensembl
Cytoband6q21
Allele length
AssemblyAllele length
hg38841
hg19841
hg18841
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv10910n54
Supporting Variantsnssv1072049
Samples
Known GenesMETTL24
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)nsv604514
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