A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv3170187



Internal ID21314248
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr1:47246596..47263416hg38UCSC Ensembl
Outerchr1:47243471..47266392hg38UCSC Ensembl
Innerchr1:47712268..47729088hg19UCSC Ensembl
Outerchr1:47709143..47732064hg19UCSC Ensembl
Innerchr1:47484855..47501675hg18UCSC Ensembl
Outerchr1:47481730..47504651hg18UCSC Ensembl
Cytoband1p33
Allele length
AssemblyAllele length
hg3822922
hg1922922
hg1822922
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv14249593, nssv14251706
SamplesSNI_12, SNI_6
Known GenesSTIL
MethodSNP array
Analysis
PlatformAffymetrix Genome-wide SNP array 6.0
Comments
ReferenceFu_et_al_2018
Pubmed ID29476164
Accession Number(s)nsv3170187
Frequency
Sample Size93
Observed Gain2
Observed Loss0
Observed Complex0
Frequencyn/a


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