A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv601942



Internal ID16389351
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr6:31607499..31664357hg38UCSC Ensembl
Innerchr6:31575276..31632134hg19UCSC Ensembl
Innerchr6:31683255..31740113hg18UCSC Ensembl
Cytoband6p21.33
Allele length
AssemblyAllele length
hg3856859
hg1956859
hg1856859
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv1154294
SamplesNINDS_50
Known GenesAIF1, APOM, BAG6, C6orf47, GPANK1, MIR6832, PRRC2A, SNORA38
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)nsv601942
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