A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv3170282



Internal ID21314343
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr1:109702376..109703659hg38UCSC Ensembl
Outerchr1:109700331..109707613hg38UCSC Ensembl
Innerchr1:110244998..110246281hg19UCSC Ensembl
Outerchr1:110242953..110250235hg19UCSC Ensembl
Innerchr1:110046521..110047804hg18UCSC Ensembl
Outerchr1:110044476..110051758hg18UCSC Ensembl
Cytoband1p13.3
Allele length
AssemblyAllele length
hg387283
hg197283
hg187283
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv14246491, nssv14244137, nssv14243086
SamplesNGO_53, NGO_20, NGO_6
Known Genes
MethodSNP array
Analysis
PlatformAffymetrix Genome-wide SNP array 6.0
Comments
ReferenceFu_et_al_2018
Pubmed ID29476164
Accession Number(s)nsv3170282
Frequency
Sample Size93
Observed Gain0
Observed Loss3
Observed Complex0
Frequencyn/a


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