A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv601967



Internal ID16389376
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr6:31903977..31909078hg38UCSC Ensembl
Innerchr6:31871754..31876855hg19UCSC Ensembl
Innerchr6:31979733..31984834hg18UCSC Ensembl
Cytoband6p21.32
Allele length
AssemblyAllele length
hg385102
hg195102
hg185102
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv10465n54
Supporting Variantsnssv1053560, nssv1053561
Samples
Known GenesC2
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)nsv601967
Frequency
Sample Size17421
Observed Gain0
Observed Loss2
Observed Complex0
Frequencyn/a


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