A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv604605



Internal ID16392014
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr6:125860810..125865328hg38UCSC Ensembl
Innerchr6:126181956..126186474hg19UCSC Ensembl
Innerchr6:126223649..126228167hg18UCSC Ensembl
Cytoband6q22.32
Allele length
AssemblyAllele length
hg384519
hg194519
hg184519
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv10926n54
Supporting Variantsnssv1072404, nssv1072405, nssv1072403
Samples
Known GenesNCOA7
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)nsv604605
Frequency
Sample Size17421
Observed Gain0
Observed Loss3
Observed Complex0
Frequencyn/a


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