A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1022500



Internal ID19111718
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr4:189413126..189618134hg38UCSC Ensembl
Innerchr4:190334280..190539288hg19UCSC Ensembl
Innerchr4:190571274..190776282hg18UCSC Ensembl
Cytoband4q35.2
Allele length
AssemblyAllele length
hg38205009
hg19205009
hg18205009
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv3636478
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)nsv1022500
Frequency
Sample Size11257
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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