A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv3169861



Internal ID21313672
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr5:6723316..6731503hg38UCSC Ensembl
Outerchr5:6720954..6735132hg38UCSC Ensembl
Innerchr5:6723429..6731616hg19UCSC Ensembl
Outerchr5:6721067..6735245hg19UCSC Ensembl
Innerchr5:6776429..6784616hg18UCSC Ensembl
Outerchr5:6774067..6788245hg18UCSC Ensembl
Cytoband5p15.31
Allele length
AssemblyAllele length
hg3814179
hg1914179
hg1814179
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv14246771
SamplesPML_1
Known GenesPAPD7
MethodSNP array
Analysis
PlatformAffymetrix Genome-wide SNP array 6.0
Comments
ReferenceFu_et_al_2018
Pubmed ID29476164
Accession Number(s)nsv3169861
Frequency
Sample Size93
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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