A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv3169882



Internal ID21313693
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr4:85820324..85848680hg38UCSC Ensembl
Outerchr4:85814461..85856504hg38UCSC Ensembl
Innerchr4:86741477..86769833hg19UCSC Ensembl
Outerchr4:86735614..86777657hg19UCSC Ensembl
Innerchr4:86960501..86988857hg18UCSC Ensembl
Outerchr4:86954638..86996681hg18UCSC Ensembl
Cytoband4q21.23
Allele length
AssemblyAllele length
hg3842044
hg1942044
hg1842044
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv14241432
SamplesPML_1
Known GenesARHGAP24
MethodSNP array
Analysis
PlatformAffymetrix Genome-wide SNP array 6.0
Comments
ReferenceFu_et_al_2018
Pubmed ID29476164
Accession Number(s)nsv3169882
Frequency
Sample Size93
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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