A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1009047



Internal ID18751578
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr4:76068027..76156732hg38UCSC Ensembl
Innerchr4:76989180..77077885hg19UCSC Ensembl
Innerchr4:77208204..77296909hg18UCSC Ensembl
Cytoband4q21.1
Allele length
AssemblyAllele length
hg3888706
hg1988706
hg1888706
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv3742871
Samples
Known GenesART3, NUP54
MethodSNP array
AnalysisAffymetrix SNP array copy number analysis
PlatformAffymetrix SNP Array 6.0
Comments
ReferenceCoe_et_al_2014
Pubmed ID25217958
Accession Number(s)nsv1009047
Frequency
Sample Size29084
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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