A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1022984



Internal ID18765517
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr4:133889406..134010749hg38UCSC Ensembl
Innerchr4:134810561..134931904hg19UCSC Ensembl
Innerchr4:135030011..135151354hg18UCSC Ensembl
Cytoband4q28.3
Allele length
AssemblyAllele length
hg38121344
hg19121344
hg18121344
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv5396n100
Supporting Variantsnssv3639531, nssv3639530
Samples
Known Genes
MethodSNP array
AnalysisAffymetrix SNP array copy number analysis
PlatformAffymetrix SNP Array 6.0
Comments
ReferenceCoe_et_al_2014
Pubmed ID25217958
Accession Number(s)nsv1022984
Frequency
Sample Size29084
Observed Gain0
Observed Loss2
Observed Complex0
Frequencyn/a


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