A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1019048



Internal ID19108265
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr4:133274617..133377744hg38UCSC Ensembl
Innerchr4:134195772..134298899hg19UCSC Ensembl
Innerchr4:134415222..134518349hg18UCSC Ensembl
Cytoband4q28.3
Allele length
AssemblyAllele length
hg38103128
hg19103128
hg18103128
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv3743109
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)nsv1019048
Frequency
Sample Size11257
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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