A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv3169884



Internal ID21313695
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr10:125407461..125421496hg38UCSC Ensembl
Outerchr10:125404278..125425349hg38UCSC Ensembl
Innerchr10:127096030..127110065hg19UCSC Ensembl
Outerchr10:127092847..127113918hg19UCSC Ensembl
Innerchr10:127086020..127100055hg18UCSC Ensembl
Outerchr10:127082837..127103908hg18UCSC Ensembl
Cytoband10q26.13
Allele length
AssemblyAllele length
hg3821072
hg1921072
hg1821072
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv14241569, nssv14243435
SamplesPML_1, SNI_6
Known Genes
MethodSNP array
Analysis
PlatformAffymetrix Genome-wide SNP array 6.0
Comments
ReferenceFu_et_al_2018
Pubmed ID29476164
Accession Number(s)nsv3169884
Frequency
Sample Size93
Observed Gain0
Observed Loss2
Observed Complex0
Frequencyn/a


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