A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv601326



Internal ID16042049
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr6:29891740..29929674hg38UCSC Ensembl
Innerchr6:29859517..29897451hg19UCSC Ensembl
Innerchr6:29967496..30005430hg18UCSC Ensembl
Cytoband6p21.33
Allele length
AssemblyAllele length
hg3837935
hg1937935
hg1837935
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv10348n54
Supporting Variantsnssv1051963, nssv1051962
Samples
Known GenesHCG4B
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)nsv601326
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