A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv3170227



Internal ID21314288
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr6:132178113..132192815hg38UCSC Ensembl
Outerchr6:132173108..132194407hg38UCSC Ensembl
Innerchr6:132499253..132513955hg19UCSC Ensembl
Outerchr6:132494248..132515547hg19UCSC Ensembl
Innerchr6:132540946..132555648hg18UCSC Ensembl
Outerchr6:132535941..132557240hg18UCSC Ensembl
Cytoband6q23.2
Allele length
AssemblyAllele length
hg3821300
hg1921300
hg1821300
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv14250674
SamplesMLY_11
Known Genes
MethodSNP array
Analysis
PlatformAffymetrix Genome-wide SNP array 6.0
Comments
ReferenceFu_et_al_2018
Pubmed ID29476164
Accession Number(s)nsv3170227
Frequency
Sample Size93
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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