A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1024786



Internal ID19114003
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr6:257341..294462hg38UCSC Ensembl
Innerchr6:257341..294462hg19UCSC Ensembl
Innerchr6:202341..239462hg18UCSC Ensembl
Cytoband6p25.3
Allele length
AssemblyAllele length
hg3837122
hg1937122
hg1837122
Variant TypeCNV gain+loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv5881n100
Supporting Variantsnssv3650474, nssv3650483, nssv3650475, nssv3650476, nssv3650484, nssv3650480, nssv3746777, nssv3650479, nssv3650481, nssv3650473, nssv3650477, nssv3650478, nssv3746778, nssv3746779, nssv3650482
Samples
Known GenesDUSP22
MethodSNP array
AnalysisAffymetrix SNP array copy number analysis
PlatformAffymetrix SNP Array 6.0
Comments
ReferenceCoe_et_al_2014
Pubmed ID25217958
Accession Number(s)nsv1024786
Frequency
Sample Size11257
Observed Gain3
Observed Loss12
Observed Complex0
Frequencyn/a


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