A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv3170077



Internal ID21314138
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr13:53055178..53072591hg38UCSC Ensembl
Outerchr13:53054660..53073157hg38UCSC Ensembl
Innerchr13:53629313..53646726hg19UCSC Ensembl
Outerchr13:53628795..53647292hg19UCSC Ensembl
Innerchr13:52527314..52544727hg18UCSC Ensembl
Outerchr13:52526796..52545293hg18UCSC Ensembl
Cytoband13q14.3
Allele length
AssemblyAllele length
hg3818498
hg1918498
hg1818498
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv14243574
SamplesNGO_24
Known Genes
MethodSNP array
Analysis
PlatformAffymetrix Genome-wide SNP array 6.0
Comments
ReferenceFu_et_al_2018
Pubmed ID29476164
Accession Number(s)nsv3170077
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