A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1067168



Internal ID19156387
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr21:18681513..18706170hg38UCSC Ensembl
Innerchr21:20053831..20078488hg19UCSC Ensembl
Innerchr21:18975702..19000359hg18UCSC Ensembl
Cytoband21q21.1
Allele length
AssemblyAllele length
hg3824658
hg1924658
hg1824658
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv4392n100
Supporting Variantsnssv3732608
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)nsv1067168
Frequency
Sample Size11257
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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