A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv601917



Internal ID16042640
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr6:31395153..31468092hg38UCSC Ensembl
Innerchr6:31362930..31435869hg19UCSC Ensembl
Innerchr6:31470909..31543848hg18UCSC Ensembl
Cytoband6p21.33
Allele length
AssemblyAllele length
hg3872940
hg1972940
hg1872940
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv10457n54
Supporting Variantsnssv1053494
Samples
Known GenesHCP5, MICA
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)nsv601917
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