A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv3169516



Internal ID21313749
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr2:114769331..114778592hg38UCSC Ensembl
Outerchr2:114756023..114778739hg38UCSC Ensembl
Innerchr2:115526908..115536169hg19UCSC Ensembl
Outerchr2:115513600..115536316hg19UCSC Ensembl
Innerchr2:115243378..115252639hg18UCSC Ensembl
Outerchr2:115230070..115252786hg18UCSC Ensembl
Cytoband2q14.1
Allele length
AssemblyAllele length
hg3822717
hg1922717
hg1822717
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv14252356
SamplesMLY_7
Known GenesDPP10
MethodSNP array
Analysis
PlatformAffymetrix Genome-wide SNP array 6.0
Comments
ReferenceFu_et_al_2018
Pubmed ID29476164
Accession Number(s)nsv3169516
Frequency
Sample Size93
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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