A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv602861



Internal ID16043584
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr6:33985869..34083140hg38UCSC Ensembl
Innerchr6:33953646..34050917hg19UCSC Ensembl
Innerchr6:34061624..34158895hg18UCSC Ensembl
Cytoband6p21.31
Allele length
AssemblyAllele length
hg3897272
hg1997272
hg1897272
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv1057870
Samples
Known GenesGRM4, MIR1275
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)nsv602861
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