A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1007692



Internal ID19096911
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr3:137311975..137324366hg38UCSC Ensembl
Innerchr3:137030817..137043208hg19UCSC Ensembl
Innerchr3:138513507..138525898hg18UCSC Ensembl
Cytoband3q22.3
Allele length
AssemblyAllele length
hg3812392
hg1912392
hg1812392
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv4904n100
Supporting Variantsnssv3608294, nssv3608285, nssv3608319, nssv3608304, nssv3608302, nssv3608318, nssv3608312, nssv3608308, nssv3608303, nssv3608293, nssv3608316, nssv3608299, nssv3607168, nssv3608288, nssv3608296, nssv3608291, nssv3608289, nssv3608297, nssv3608309, nssv3608300, nssv3608311, nssv3608283, nssv3608298, nssv3608290, nssv3608314, nssv3608295, nssv3608286, nssv3607171, nssv3608317, nssv3608284, nssv3608306, nssv3607170, nssv3607172, nssv3608292, nssv3607167, nssv3608301, nssv3608305, nssv3607173, nssv3608307, nssv3608287, nssv3608313, nssv3608282, nssv3607169, nssv3608315, nssv3608310, nssv3608281
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)nsv1007692
Frequency
Sample Size11257
Observed Gain0
Observed Loss46
Observed Complex0
Frequencyn/a


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