A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1050640



Internal ID19139859
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr13:70168184..70198751hg38UCSC Ensembl
Innerchr13:70742316..70772883hg19UCSC Ensembl
Innerchr13:69640317..69670884hg18UCSC Ensembl
Cytoband13q21.33
Allele length
AssemblyAllele length
hg3830568
hg1930568
hg1830568
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv1712n100
Supporting Variantsnssv3529353, nssv3529351, nssv3529354, nssv3529364, nssv3713234, nssv3529349, nssv3713233, nssv3529365, nssv3529348, nssv3529350, nssv3529362, nssv3529367, nssv3529366, nssv3529360, nssv3529355, nssv3529356, nssv3529361, nssv3713232, nssv3529363, nssv3529359, nssv3529352, nssv3529358, nssv3713235, nssv3529368, nssv3529357
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)nsv1050640
Frequency
Sample Size11257
Observed Gain0
Observed Loss25
Observed Complex0
Frequencyn/a


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