A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1013808



Internal ID19103027
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr1:49448439..49532002hg38UCSC Ensembl
Innerchr1:49914111..49997674hg19UCSC Ensembl
Innerchr1:49686698..49770261hg18UCSC Ensembl
Cytoband1p33
Allele length
AssemblyAllele length
hg3883564
hg1983564
hg1883564
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv163n100
Supporting Variantsnssv3467333, nssv3479717, nssv3475938, nssv3700665, nssv3466474, nssv3467429
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)nsv1013808
Frequency
Sample Size11257
Observed Gain0
Observed Loss6
Observed Complex0
Frequencyn/a


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