A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv3170082



Internal ID21314143
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr4:121360818..121363980hg38UCSC Ensembl
Outerchr4:121353499..121369976hg38UCSC Ensembl
Innerchr4:122281973..122285135hg19UCSC Ensembl
Outerchr4:122274654..122291131hg19UCSC Ensembl
Innerchr4:122501423..122504585hg18UCSC Ensembl
Outerchr4:122494104..122510581hg18UCSC Ensembl
Cytoband4q27
Allele length
AssemblyAllele length
hg3816478
hg1916478
hg1816478
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv14249326, nssv14252238
SamplesMLY_17, PML_1
Known GenesQRFPR
MethodSNP array
Analysis
PlatformAffymetrix Genome-wide SNP array 6.0
Comments
ReferenceFu_et_al_2018
Pubmed ID29476164
Accession Number(s)nsv3170082
Frequency
Sample Size93
Observed Gain0
Observed Loss2
Observed Complex0
Frequencyn/a


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