A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1022438



Internal ID19111656
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr4:149145197..149275559hg38UCSC Ensembl
Innerchr4:150066349..150196711hg19UCSC Ensembl
Innerchr4:150285799..150416161hg18UCSC Ensembl
Cytoband4q31.23
Allele length
AssemblyAllele length
hg38130363
hg19130363
hg18130363
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv3636073
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)nsv1022438
Frequency
Sample Size11257
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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