A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1009003



Internal ID19098221
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr1:49449248..49532002hg38UCSC Ensembl
Innerchr1:49914920..49997674hg19UCSC Ensembl
Innerchr1:49687507..49770261hg18UCSC Ensembl
Cytoband1p33
Allele length
AssemblyAllele length
hg3882755
hg1982755
hg1882755
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv163n100
Supporting Variantsnssv3462924, nssv3700669, nssv3471524, nssv3467471, nssv3465404, nssv3481154, nssv3480289, nssv3473153, nssv3477057, nssv3466595, nssv3475874
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)nsv1009003
Frequency
Sample Size11257
Observed Gain0
Observed Loss11
Observed Complex0
Frequencyn/a


Hosted by The Centre for Applied Genomics
Grant support for DGV
Please read the usage disclaimer