A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1011119



Internal ID19100336
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr1:49177942..49289300hg38UCSC Ensembl
Innerchr1:49643614..49754972hg19UCSC Ensembl
Innerchr1:49416201..49527559hg18UCSC Ensembl
Cytoband1p33
Allele length
AssemblyAllele length
hg38111359
hg19111359
hg18111359
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv3471127
Samples
Known GenesAGBL4
MethodSNP array
AnalysisAffymetrix SNP array copy number analysis
PlatformAffymetrix SNP Array 6.0
Comments
ReferenceCoe_et_al_2014
Pubmed ID25217958
Accession Number(s)nsv1011119
Frequency
Sample Size11257
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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