A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv999834



Internal ID19159370
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr3:65203548..65230894hg38UCSC Ensembl
Innerchr3:65189223..65216569hg19UCSC Ensembl
Innerchr3:65164263..65191609hg18UCSC Ensembl
Cytoband3p14.1
Allele length
AssemblyAllele length
hg3827347
hg1927347
hg1827347
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv4762n100
Supporting Variantsnssv3593865, nssv3593838, nssv3593848, nssv3593858, nssv3593849, nssv3593842, nssv3593843, nssv3593854, nssv3593853, nssv3593845, nssv3593867, nssv3593851, nssv3593855, nssv3593837, nssv3593840, nssv3593856, nssv3593850, nssv3593861, nssv3593862, nssv3593839, nssv3593846, nssv3593860, nssv3593852, nssv3593857, nssv3593864, nssv3593866, nssv3593841, nssv3593863, nssv3593844, nssv3593847, nssv3593859, nssv3593836
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)nsv999834
Frequency
Sample Size11257
Observed Gain0
Observed Loss32
Observed Complex0
Frequencyn/a


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